K170228 · Belimed AG · FLE · May 12, 2017 · General Hospital
Device Facts
Record ID
K170228
Device Name
Belimed Steam Sterilizer MST-H TOP 5000
Applicant
Belimed AG
Product Code
FLE · General Hospital
Decision Date
May 12, 2017
Decision
SESE
Submission Type
Abbreviated
Regulation
21 CFR 880.6880
Device Class
Class 2
Attributes
Therapeutic
Indications for Use
The Belimed Steam Sterilizer TOP 5000 is designed for sterilization of non-porous and porous heat and moisture stable materials used in healthcare facilities.
Device Story
Steam sterilizer for healthcare facilities; processes non-porous and porous heat/moisture-stable materials. Inputs: instrument trays or fabric packs loaded into chamber. Operation: uses steam as sterilizing agent; factory-programmed cycles (Prevacuum, Gravity, Liquid, Bowie-Dick, Leak Test) controlled by PLC. Outputs: sterilized medical materials; cycle documentation via matrix dot printer. Used in clinical settings; operated by trained personnel. Benefits: ensures sterility of surgical instruments and materials, reducing infection risk. Performance verified via AAMI ST8:2013 standards, including sterility assurance level (SAL) validation and moisture retention testing.
Clinical Evidence
No clinical data required. Bench testing only. Validation performed per ANSI/AAMI ST8:2013. Prevac and Immediate Use Gravity cycles qualified for 25 lb tray capacity; demonstrated SAL of at least 10^-6, F0 >= 12 minutes, and moisture retention < 20%.
Technological Characteristics
Chamber/piping: 316L stainless steel. Energy: Steam, 3-phase 208V 60Hz. Control: PLC with 5.7" LCD HMI. Connectivity: Matrix dot printer. Safety: ASME-approved pressure relief valves. Air filtration: 0.3 microns. Standards: ANSI/AAMI ST8:2013, ST79, IEC 61010-2-040, UL 61010-1, ASME Section VIII Div 1.
Indications for Use
Indicated for sterilization of non-porous and porous heat and moisture stable materials in healthcare facilities.
Regulatory Classification
Identification
A steam sterilizer (autoclave) is a device that is intended for use by a health care provider to sterilize medical products by means of pressurized steam.
Predicate Devices
Belimed Steam Sterilizer TOP 5000 Series 9-18 (K021223)
Submission Summary (Full Text)
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Image /page/0/Picture/2 description: The image shows the logo for the Department of Health & Human Services - USA. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized image of three human profiles facing to the right, stacked on top of each other.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
May 12, 2017
Belimed AG Jay Upchurch Product Engineer, U.S. Agent Belimed. Inc. 2325 Charleston Regional Parkway Charleston, South Carolina 29412
Re: K170228
Trade/Device Name: Belimed Steam Sterilizer MST-H TOP 5000 Regulation Number: 21 CFR 880.6880 Regulation Name: Steam Sterilizer Regulatory Class: Class II Product Code: FLE Dated: April 6, 2017 Received: April 12, 2017
Dear Jay Upchurch:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR
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Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely.
# Michael J. Ryan -S
for Tina Kiang, Ph.D. Acting Director Division of Anesthesiology. General Hospital, Respiratory, Infection Control, and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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### Indications for Use
510(k) Number (if known) K170228
Device Name Belimed Steam Sterilizer MST-H TOP 5000
Indications for Use (Describe)
The Belimed Steam Sterilizer TOP 5000 is designed for sterilization of non-porous and porous heat and moisture stable materials used in healthcare facilities.
The Belimed Steam Sterilizer MST-H TOP 5000 is equipped with the following factory programmed sterilization cycles and cycle values. This is shown in Table 1.
| Type of Use (Select one or both, as applicable) | |
|-----------------------------------------------------------------------|---------------------------------------------------------------------------------|
| <input type="checkbox"/> Prescription Use (Part 21 CFR 801 Subpart D) | <input checked="" type="checkbox"/> Over-The-Counter Use (21 CFR 801 Subpart C) |
|X | Over-The-Counter Use (21 CFR 801 Subpart C)
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# Table 1: Factory programmed sterilization cycles and cycle values.
| CYCLES | STERILIZE<br>TEMP | STERILIZE<br>TIME | DRY<br>TIME | RECOMMENDED LOAD |
|-----------------------------------------------|-------------------|-------------------|-------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| PREVAC 270F<br>(132°C) | 270°F<br>(132°C) | 4 minutes | 30 minutes | Double-wrapped instrument trays.<br>Maximum weight of 25 lbs. each for the following models: 9-6-12 HS2, 9-6-15 HS1, and GR 9-6-18 HS2.<br>Maximum weight of 17 lbs. each for the following models: 9-6-9 HS1, 9-6-9 HS2, 9-6-12 HS1, 9-6-15 HS2, 9-6-18 HS1, 9-6-18 HS2, GR 9-6-9 HS1, GR 9-6-9 HS2, GR 9-6-12 HS1, GR 9-6-12 HS2, GR 9-6-15 HS1, GR 9-6-15 HS2, GR 9-6-15 HS2, GR 9-6-18 HS1.<br>Fabric Packs. |
| PreVac 270F 4S<br>/ 5Dry (132°C) | 270°F<br>(132°C) | 4 minutes | 5 minutes | Fabric Packs. |
| Liquid 250F<br>(121°C) | 250°F<br>(121°C) | 45 minutes | 0 minute | Max 1000 ml of Liquid per bottle. Use only vented bottles, type I, borosilicate glass. |
| Express 270F<br>(132°C) | 270°F<br>(132°C) | 4 minutes | 3 minutes | Single wrapped instrument tray with non-porous single instrument. |
| Immediate Use<br>270F - Single Ins<br>(132°C) | 270°F<br>(132°C) | 3 minutes | 1 minute | Unwrapped instrument tray with a single instrument. |
| Immediate Use<br>270F - Multi Ins<br>(132°C) | 270°F<br>(132°C) | 10 minutes | 1 minute | Unwrapped instrument tray with non-porous multiple instruments.<br>Maximum weight of 25 lbs each for the following models: 9-6-12 HS2, 9-6-15 HS1, and GR 9-6-18 HS2.<br>Maximum weight of 17 lbs. each for the following models: 9-6-9 HS1, 9-6-9 HS2, 9-6-12HS1, 9-6-15 HS2, 9-6-18 HS1, 9-6-18 HS2, GR 9-6-9 HS1, GR 9-6-9 HS2, GR 9-6-12 HS1, GR 9-6-12 HS2, GR 9-6-15 HS1, GR 9-6-15 HS1, GR 9-6-15 HS2, GR 9-6-18 HS1. Maximum of 4 instrument trays. |
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# 510(k) Summary
K170228
#### Date: May 5, 2017 Owner's Name / Address: Belimed AG Grienbachstrasse 11 CH-6300 Zug / Switzerland Preparer's Name / Address: Belimed, Inc. 2325 Charleston Regional Parkway Charleston, SC 29412 USA Contact Person: Jay Upchurch Email: Jay.Upchurch@Belimed.com Phone: (843) 216-7424 x133 (843) 216-7707 Fax: Trade Name: Belimed Steam Sterilizer MST-H TOP 5000 9-6-9 HS1, 9-6-9 HS2, 9-6-12 HS1, 9-6-12 Models: HS2, 9-6-15 HS1, 9-6-15 HS2, 9-6-18 HS1, 9-6-18 HS2, GR 9-6-9 HS1, GR 9-6-9 HS2, GR 9-6-12 HS1, GR 9-6-12 HS2, GR 9-6-15 HS1, GR 9-6-15 HS2, GR 9-6-18 HS1, and GR 9-6-18 HS2. Classification: Steam Sterilizer - Class II, as listed per 21 CFR 880.6880 Product Code: FLE Predicate Device: Belimed Steam Sterilizer TOP 5000 Series 9-18 (K021223)
### INTENDED USE:
The Belimed Steam Sterilizer TOP 5000 is designed for sterilization of non-porous and porous heat and moisture stable materials used in healthcare facilities.
The Belimed Steam Sterilizer MST-H TOP 5000 is equipped with the following factory programmed sterilization cycles and cycle values. This is shown in Table 1.
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# Table 1: Factory programmed sterilization cycles and cycle values.
| CYCLES | STERILIZE<br>TEMP | STERILIZE<br>TIME | DRY<br>TIME | RECOMMENDED LOAD |
|-----------------------------------------------|-------------------|-------------------|---------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| PREVAC 270F<br>(132°C) | 270°F<br>(132°C) | 4 minutes | 30<br>minutes | Double-wrapped instrument trays.<br>Maximum weight of 25 lbs. each for the following models: 9-<br>6-12 HS2, 9-6-15 HS1, and GR 9-6-18 HS2.<br>Maximum weight of 17 lbs. each for the following models: 9-<br>6-9 HS1, 9-6-9 HS2, 9-6-12 HS1, 9-6-15 HS2, 9-6-18 HS1,<br>9-6-18 HS2, GR 9-6-9 HS1, GR 9-6-9 HS2, GR 9-6-12 HS1,<br>GR 9-6-12 HS2, GR 9-6-15 HS1, GR 9-6-15 HS1, GR 9-6-<br>15 HS2, GR 9-6-18 HS1.<br>Fabric Packs. |
| PreVac 270F 4S<br>/ 5Dry (132ºC) | 270°F<br>(132°C) | 4 minutes | 5<br>minutes | Fabric Packs. |
| Liquid 250F<br>(121°C) | 250°F<br>(121°C) | 45 minutes | 0<br>minute | Max 1000 ml of Liquid per bottle. Use only vented bottles,<br>type I, borosilicate glass. |
| Express 270F<br>(132°C) | 270°F<br>(132°C) | 4 minutes | 3<br>minutes | Single wrapped instrument tray with non-porous single<br>instrument. |
| Immediate Use<br>270F - Single Ins<br>(132°C) | 270°F<br>(132°C) | 3 minutes | 1<br>minute | Unwrapped instrument tray with a single instrument. |
| Immediate Use<br>270F - Multi Ins<br>(132°C) | 270°F<br>(132°C) | 10 minutes | 1<br>minute | Unwrapped instrument tray with non-porous multiple<br>instruments.<br>Maximum weight of 25 lbs each for the following models: 9-<br>6-12 HS2, 9-6-15 HS1, and GR 9-6-18 HS2.<br>Maximum weight of 17 lbs. each for the following models: 9-<br>6-9 HS1, 9-6-9 HS2, 9-6-12HS1, 9-6-15 HS2, 9-6-18 HS1,<br>9-6-18 HS2, GR 9-6-9 HS1, GR 9-6-9 HS2, GR 9-6-12 HS1,<br>GR 9-6-12 HS2, GR 9-6-15 HS1, GR 9-6-15 HS1, GR 9-6-<br>15 HS2, GR 9-6-18 HS1. Maximum of 4 instrument trays. |
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# DESCRIPTION OF DEVICE:
The Belimed Steam Sterilizers MST-H, models 9-6-9, 9-6-12, 9-6-15, and 9-6-18 are available in a single door (HS1) or double door (HS2) version. The sterilizers are available in a carriage loader and a ground loader (GR) version.
The sterilizers are equipped with Prevacuum, Gravity, Liquid, Air Leak Test and Bowie-Dick Test cycles.
The Belimed Steam Sterilizers TOP 5000 are equipped with the following predefined cycles (Table 2):
Table 2: Factory programmed sterilization and test cycles.
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| No. | CYCLE | PRE-<br>TREATMENT | STERILIZE<br>TEMP | STERILIZE<br>TIME | DRY<br>TIME | RECOMMENDED LOAD |
|-----|---------------------------------------|--------------------------------------------|-------------------|-------------------|---------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| 1 | PreVac 270F<br>4S / 30Dry | 4 pulses | 270°F | 4 minutes | 30<br>minutes | Double-wrapped instrument trays.<br>Maximum weight of 25 lbs each for the<br>following models: 9-6-12 HS2, 9-6-15<br>HS1, and GR 9-6-18 HS2.<br>Maximum weight of 17 lbs. each for the<br>following models: 9-6-9 HS1, 9-6-9 HS2,<br>9-6-12 HS1, 9-6-15 HS2, 9-6-18 HS1, 9-6-18 HS2, GR 9-6-9 HS1, GR 9-6-9 HS2,<br>GR 9-6-12 HS1, GR 9-6-12 HS2, GR 9-6-15 HS1, GR 9-6-15 HS2, GR 9-6-18 HS1.<br>Fabric Packs. |
| 2 | PreVac 270F<br>4S / 5Dry | 4 pulses | 270°F | 4 minutes | 5<br>minutes | Fabric Packs. |
| 3 | Immediate<br>Use 270F -<br>Single Ins | Purge | 270°F | 3 minutes | 1 minute | Unwrapped instrument tray with a single<br>instrument |
| 4 | Immediate<br>Use 270F -<br>Multi Ins | Purge | 270°F | 10 minutes | 1 minute | Unwrapped instrument tray with non<br>porous multiple instruments.<br>Maximum weight of 25 lbs each for the<br>following models: 9-6-12 HS2, 9-6-15<br>HS1, and GR 9-6-18 HS2.<br>Maximum weight of 17 lbs. each for the<br>following models: 9-6-9 HS1, 9-6-9 HS2,<br>9-6-12HS1, 9-6-15 HS2, 9-6-18 HS1, 9-6-18 HS2, GR 9-6-9 HS1, GR 9-6-9 HS2,<br>GR 9-6-12 HS1, GR 9-6-12 HS2, GR 9-6-15 HS1, GR 9-6-15 HS2, GR 9-6-15 HS2,<br>GR 9-6-18 HS1. Maximum of 4<br>instrument trays. |
| 5 | Express 270F | 2 pulses | 270°F | 4 minutes | 3<br>minutes | Single wrapped instrument tray with non<br>porous single instrument |
| 6 | Bowie-Dick<br>Test | 4 pulses | 273°F | 3.5 minutes | 1 minute | One DART or Bowie-Dick-Test-Pack |
| 7 | Leak Test | Vacuum:<br>65 mbar<br>Test time:<br>15 min | - | - | - | Empty chamber |
| 8 | Warm up &<br>Leak Test | Vacuum:<br>65 mbar<br>Test time:<br>15 min | 270°F | 4 minutes | 3<br>minutes | Empty chamber |
| 10 | Liquid 250F | Purge | 250°F | 45 minutes | Max 1000 ml of Liquid per bottle. Use only vented bottles, type I, borosilicate glass<br>Cycle disabled | |
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Notes on Table 2:
1. Factory set sterilize time is recommended.
2. Factory set dry time.
3. Recommended load: Refer to table 4 and 5.
4. Fabric load should be preconditioned between 68°F and 75°F and at a relative humidity of at least 35% to 60% for at least 2 hours.
5. The liquid cycle is for non-patient contact use only.
The Belimed Steam Sterilizers MST-H are offered in the following versions:
| Model<br>Single Door<br>Double Door | Configuration | Chamber Size (H x W x D) (mm) | Overall Size (H x W x D) (mm) |
|-------------------------------------|---------------|-------------------------------|-------------------------------|
| 9-6-9 HS1 | 1 door | 1080 x 660 x 1040 | 2000 x 1700 x 1280 |
| GR 9-6-9 HS1 | | 1230 x 660 x 1100 | 2000 x 1900 x 1600 |
| 9-6-9 HS2 | 2 door | 1080 x 660 x 1040 | 2000 x 1700 x 1300 |
| GR 9-6-9 HS2 | | 1230 x 660 x 1100 | 2000 x 1900 x 1600 |
| 9-6-12 HS1 | 1 door | 1080 x 660 x 1398 | 1970 x 1700 x 1714 |
| GR 9-6-12 HS1 | | 1230 x 660 x 1400 | 2000 x 1900 x 1900 |
| 9-6-12 HS2 | 2 door | 1080 x 660 x 1398 | 1970 x 1700 x 1714 |
| GR 9-6-12 HS2 | | 1230 x 660 x 1400 | 2000 x 1900 x 1900 |
| 9-6-15 HS1 | 1 door | 1080 x 660 x 1700 | 1970 x 1700 x 2022 |
| GR 9-6-15 HS1 | | 1230 x 660 x 1706 | 2000 x 1900 x 2200 |
| 9-6-15 HS2 | 2 door | 1080 x 660 x 1700 | 1970 x 1700 x 2022 |
| GR 9-6-15 HS2 | | 1230 x 660 x 1706 | 2000 x 1900 x 2200 |
| 9-6-18 HS1 | 1 door | 1080 x 660 x 2014 | 1970 x 1700 x 2330 |
| GR 9-6-18 HS1 | | 1230 x 660 x 2000 | 2000 x 1900 x 2500 |
| 9-6-18 HS2 | 2 door | 1080 x 660 x 2014 | 1970 x 1700 x 2330 |
| GR 9-6-18 HS2 | | 1230 x 660 x 2000 | 2000 x 1900 x 2500 |
Table 3. Versions and dimensions.
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The following tables show the recommended loads for the Belimed Steam Sterilizers MST-H:
| Sterilizer Chamber Size (mm) | Model | Wrapped Instrument Trays 20"x10" max. 17lb each | Fabric Packs 11"x11"x9" max 6.6lb each | Fabric Packs 23"x11"x11" max. 17lb each |
|-------------------------------------|---------------------------------|-------------------------------------------------|----------------------------------------|-----------------------------------------|
| 26"x 42.5"x 41" (660 x 1080 x 1040) | 9-6-9 HS1 and 9-6-9 HS2 | 9 | 18 | 9 |
| 26"x 42.5"x 55" (660 x 1080 x 1400) | 9-6-12 HS1 | 12 | 30 | 12 |
| 26"x 42.5"x 67" (660 x 1080 x 1700) | 9-6-15 HS2 | 15 | 36 | 15 |
| 26"x 42.5"x 79" (660 x 1080 x 2000) | 9-6-18 HS1 and 9-6-18 HS2 | 18 | 42 | 18 |
| 26"x 48.5"x 43" (660 x 1230 x 1100) | GR 9-6-9 HS1 and GR 9-6-9 HS2 | 9 | 18 | 9 |
| 26"x 48.5"x 55" (660 x 1230 x 1400) | GR 9-6-12 HS1 and GR 9-6-12 HS2 | 12 | 30 | 12 |
| 26"x 48.5"x 67" (660 x 1230 x 1700) | GR 9-6-15 HS1 and GR 9-6-15 HS2 | 15 | 36 | 15 |
| 26"x 48.5"x 79" (660 x 1230 x 2000) | GR 9-6-18 HS1 | 18 | 42 | 18 |
Table 4: Recommended loads by sterilizer for 17 lb. instrument trays and fabric packs.
Table 5: Recommended loads by sterilizer for 25 lb. instrument trays and fabric packs.
| Sterilizer Chamber Size<br>(mm) | Model | Wrapped<br>Instrument<br>Trays 20"x10"<br>max. 25 lb.<br>each | Fabric<br>Packs<br>11"x11"x9"<br>max 6.6lb<br>each | Fabric<br>Packs<br>23"x11"x11"<br>max. 17lb<br>each |
|----------------------------------------|---------------|---------------------------------------------------------------|----------------------------------------------------|-----------------------------------------------------|
| 26"x 42.5"x 55" (660 x 1080<br>x 1400) | 9-6-12 HS2 | 12 | 30 | 12 |
| 26"x 42.5"x 67" (660 x 1080<br>x 1700) | 9-6-15 HS1 | 15 | 36 | 15 |
| 26"x 48.5"x 79" (660 x 1230<br>x 2000) | GR 9-6-18 HS2 | 18 | 42 | 18 |
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| Model | Volume of Liquid in One<br>Container | Number of Containers |
|-----------|--------------------------------------|----------------------|
| 9-6-9 | 1000 mL | 126 |
| GR 9-6-9 | 1000 mL | 126 |
| 9-6-12 | 1000 mL | 168 |
| GR 9-6-12 | 1000 mL | 168 |
| 9-6-15 | 1000 mL | 210 |
| GR 9-6-15 | 1000 mL | 210 |
| 9-6-18 | 1000 mL | 252 |
| GR 9-6-18 | 1000 mL | 252 |
Table 6. Recommended loads for liquid cycle 250F.
The Belimed Steam Sterilizer TOP 5000 is designed for sterilization of non-porous and porous heat and moisture stable materials used in healthcare facilities.
The Belimed Steam Sterilizer TOP 5000 is offered in the following medium-size configurations:
26"x 42.5"x 41" (660 mm x 1080 mm x 1040 mm) Single Door, Prevacuum 26"x 42.5"x 41" (660 mm x 1080 mm x 1040 mm) Double Door, Prevacuum 26"x 42.5"x 55" (660 mm x 1080 mm x 1400 mm) Single Door, Prevacuum 26"x 42.5"x 55" (660 mm x 1080 mm x 1400 mm) Double Door, Prevacuum 26"x 42.5"x 67" (660 mm x 1080 mm x 1700 mm) Single Door, Prevacuum 26"x 42.5"x 67" (660 mm x 1080 mm x 1700 mm) Double Door, Prevacuum 26"x 42.5"x 79" (660 mm x 1080 mm x 2000 mm) Single Door, Prevacuum 26"x 42.5"x 79" (660 mm x 1080 mm x 2000 mm) Double Door, Prevacuum 26"x 48.5"x 43" (660 mm x 1230 mm x 1100 mm) Single Door, Floor Flush Design, Prevacuum 26"x 48.5"x 43" (660 mm x 1230 mm x 1100 mm) Double Door, Floor Flush Design, Prevacuum 26"x 48.5"x 55" (660 mm x 1230 mm x 1400 mm) Single Door, Floor Flush Design, Prevacuum 26"x 48.5"x 55" (660 mm x 1230 mm x 1400 mm) Double Door, Floor Flush Design, Prevacuum 26"x 48.5"x 67" (660 mm x 1230 mm x 1700 mm) Single Door, Floor Flush Design, Prevacuum 26"x 48.5"x 67" (660 mm x 1230 mm x 1700 mm) Double Door, Floor Flush Design, Prevacuum 26"x 48.5"x 79" (660 mm x 1230 mm) Single Door, Floor Flush Design, Prevacuum 26"x 48.5"x 79" (660 mm x 1230 mm) Double Door, Floor Flush Design, Prevacuum
The Belimed Steam Sterilizers MST-H, models 9-6-9 HS1, 9-6-9 HS2, 9-6-12 HS1, 9-6-12 HS2, 9-6-15 HS1, 9-6-15 HS2, 9-6-18 HS1, 9-6-18 HS2, GR 9-6-9 HS1, GR 9-6-9 HS2, GR 9-6-12 HS1, GR 9-6-12 HS2, GR 9-6-15 HS1, GR 9-6-15 HS2, GR 9-6-18 HS1, and GR 9-6-18 HS2 are designed for the sterilization of non-porous and porous heat and moisture stable materials used in healthcare facilities.
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# NONCLINICAL COMPARISON TO THE PREDICATE DEVICE:
The Belimed Steam Sterilizers MST-H, models 9-6-9, 9-6-12, 9-6-15, and 9-6-18 are very similar to the predicate device.
A summary of the differences to the predicate device is included in Table 7.
| General Sterilizer<br>Features | Belimed Steam Sterilizer<br>TOP 5000 Series 9-18<br>(K021223) | Belimed Steam<br>Sterilizer TOP 5000<br>Series 9-18 | Comparison |
|------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------|
| Intended Use | Terminal Sterilization of non-<br>porous and porous heat and<br>moisture-stable materials<br>used in healthcare facilities | Terminal Sterilization<br>of non-porous and<br>porous heat and<br>moisture-stable<br>materials used in<br>healthcare facilities | Same |
| Operating<br>principle | The sterilizing agent is<br>steam. | The sterilizing agent<br>is steam. | Same |
| Built according to<br>standard | ANSI/AAMI ST8:1994<br>Hospital Steam Sterilizers | ANSI/AAMI ST8:2013<br>Hospital Steam<br>Sterilizers | Same |
| Chamber sizes | (H x W x D) in mm: | (H x W x D) in mm: | Same |
| Model:<br>9-6-9 / 9-6-12 /<br>GR9-6-12<br>9-6-15 / GR9-6-<br>15<br>9-6-18 / GR9-6-<br>18 | 1080x660x1040<br>1080x660x1400 /<br>1230x660x1400<br>1080x660x1700 /<br>1230x660x1700<br>1080x660x2000 /<br>1230x660x2000 | 1080x660x1040<br>1080x660x1400 /<br>1230x660x1400<br>1080x660x1700 /<br>1230x660x1700<br>1080x660x2000 /<br>1230x660x2000 | Same |
| Sterilization<br>cycles | PreVac 270 °F<br>Gravity 270 °F<br>Liquid 250 °F<br>Bowie Dick Test<br>Air Leak Test | PreVac 270 °F<br>Gravity 270 °F<br>Liquid 250 °F<br>Bowie Dick Test<br>Air Leak Test | Same |
| Max. instrument<br>tray weight | 17 lbs. | 17 lbs. for 9-6-9 HS1<br>9-6-9 HS2, GR 9-6-9<br>HS1, GR 9-6-9 HS2,<br>9-6-12 HS1, GR 9-6-<br>12HS1,<br>9-6-15 HS2, GR 9-6-<br>15 HS1, GR 9-6-15<br>HS2, 9-6-18 HS1, 9- | Same |
| 6-18 HS2, GR 9-6-18<br>HS1 | | | |
| 25 lbs. for 9-6-12<br>HS2, 9-6-15 HS1,<br>and GR 9-6-18 HS2 | | | |
| Load capacity<br>instrument trays | | | |
| Model: | | | |
| 9-6-9 / 9-6-12 /<br>GR9-6-12 | 9 | 9 | Same |
| 9-6-15 / GR9-6- | 12 | 12 | |
| 15 | 15 | 15 | |
| 9-6-18 / GR9-6-<br>18 | 18 | 18 | |
| Chamber<br>material | Stainless steel 316L | Stainless steel 316L | Same |
| Chamber design<br>pressure | 39 psi | 39 psi | Same |
| Door construction | Automated horizontal sliding<br>door(s) | Automated horizontal<br>sliding door(s) | Same |
| Safety (pressure<br>relief) valves | ASME approved | ASME approved | Same |
| Piping | Stainless steel 316 L | Stainless steel 316 L | Same |
| Electrical | 3 phase 208V 60Hz | 3 phase 208V 60Hz | Same |
| HMI Technology | LCD color / 5.7" | LCD color / 5.7" | Same |
| Control<br>Technology | PLC | PLC | Same |
| Printer<br>Technology | Matrix Dot Technology | Matrix Dot<br>Technology | Same |
| Vacuum pump | 9-6-9 / GR 9-6-9: 95m3/h<br><br>9-6-12 / GR 9-6-12: 95m3/h<br><br>9-6-15 / GR 9-6-15: 130m3/h<br><br>9-6-18 / GR 9-6-18: 130m3/h | 9-6-9 / GR 9-6-9:<br>95m3/h<br><br>9-6-12 / GR 9-6-12:<br>95m3/h<br><br>9-6-15 / GR 9-6-15:<br>130m3/h<br><br>9-6-18 / GR 9-6-18:<br>130m3/h | Same |
| Air filter | 0.3 microns | 0.3 microns | Same |
Table 7. A summary of the differences to the predicate device.
{12}------------------------------------------------
{13}------------------------------------------------
## CLINICAL DATA:
No clinical data is required for this device classification submission.
### SUMMARY OF PERFORMANCE TESTING:
Belimed validates its sterilization cycles by recommended practices, standards and quidelines developed by various independent organizations such as the Association for Advancement of Medical Instrumentation (AAMI). Prior to release, Belimed Steam Sterilizer MST-H were validated to meet the requirements of ANSI/AAMI ST8:2013.
The results of the Belimed Steam Sterilizer MST-H verification studies demonstrate that the sterilizer performs as intended and is summarized as follows:
- The Prevac cycle where the maximum tray capacity is changing to 25 lbs. was qualified according to AAMI ST8:2013 section 5.5.4. This cycle demonstrated a sterility assurance level of at least 10° through achievement of a time-at-temperature sufficient to produce an F0 of at least 12 minutes by half cycle, moisture retention of less than 20% increase in pre-sterilization weight of the towel, and exhibited no wet spots on the outer wrapper.
- The Immediate Use Gravity cycle where the maximum tray capacity is changing from 17 lbs. to 25 lbs. was qualified according to AAMI ST8:2013 section 5.5.5.1.
# STANDARDS USED:
Belimed's sterilizers, including the Belimed Steam Sterilizer MST-H, models 9-6-12, and 9-6-18, have been designed and constructed to meet the safety and performance requirements of various national safety codes and standards. The Belimed Steam Sterilizer MST-H complies with the following safety standards:
- 1. ANSI/AAMI ST8:2013
- 2. ANSI/AAMI ST79:2010+A1:2010
- 3. IEC EN 62304:2006
- 4. EN ISO 14971:2012
- ISO 13485:2012 Medical Devices Quality management systems. Requirements for 5. regulatory purposes
- 6. IEC EN 60601-1-2:2007
- American Society of Mechanical Engineers (ASME), Section VIII, Division 1 for unfired 7. pressure vessels Ed. 2015.
- 8. UL 61010-1:2004 Safety requirements for electrical equipment for measurement, control and laboratory use -Part 1: General requirements.
- 9. IEC 61010-2-040:2005 Safety requirements for electrical equipment for measurement, control and laboratory use -Part 2: Particular requirements for sterilizers and washerdisinfectors used to treat medical materials.
{14}------------------------------------------------
# CONCLUSION
The Belimed Steam Sterilizer MST-H Top 5000 is substantially equivalent device to that of the predicate device (K021223).
The nonclinical tests and accompanying in this premarket notification demonstrate that this device is as safe, as effective, and performs as well or better than the predicate device series (K021223).
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Learn the FDA Browser
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.