← Product Code [LZA](/productcode/LZA) · K122727 # BLUE STERILE POWDER FREE NITRILE EXAMINATION GLOVE (K122727) _Northstar Healthcare Holdings · LZA · Feb 22, 2013 · General Hospital · SESE_ **Canonical URL:** https://fda-staging.innolitics.com/device/K122727 ## Device Facts - **Applicant:** Northstar Healthcare Holdings - **Product Code:** [LZA](/productcode/LZA.md) - **Decision Date:** Feb 22, 2013 - **Decision:** SESE - **Submission Type:** Abbreviated - **Regulation:** 21 CFR 880.6250 - **Device Class:** Class 1 - **Review Panel:** General Hospital - **Attributes:** 3rd-Party Reviewed ## Indications for Use The Textured Blue Sterile Powder Free Nitrile Examination Gloves is a Disposable device intended for medical and dental purposes to be worn on the examiner's hand or finger to prevent contamination between patient and examiner. ## Device Story Textured Blue Sterile Powder Free Nitrile Examination Gloves; disposable nitrile gloves; worn on examiner's hand or finger; prevents contamination between patient and examiner; used in medical and dental settings; sterile; powder-free; provided in small, medium, and large sizes; single-use; physical properties meet ASTM standards; biocompatible; non-irritating; no sensitization potential. ## Clinical Evidence Bench testing only. Device performance verified against ASTM D6319-10 (dimensions, physical properties), ASTM D5151-06 (pinholes), and ASTM D6124-06 (residual powder). Biocompatibility testing performed per ISO 10993-10:2010, confirming non-irritating and non-sensitizing properties. ## Technological Characteristics Nitrile material; sterile; powder-free; textured surface; dimensions per ASTM D6319-10; physical properties (tensile strength 14MPa, elongation 500% before aging) per ASTM D6319-10; pinhole resistance per ASTM D5151-06; residual powder <2mg per ASTM D6124-06; biocompatibility per ISO 10993-10:2010. ## Regulatory Identification A non-powdered patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner. A non-powdered patient examination glove does not incorporate powder for purposes other than manufacturing. The final finished glove includes only residual powder from manufacturing. ## Predicate Devices - Sterile Nitrile Powder Free Examination Gloves ([K081466](/device/K081466.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ K122727 Abbreviated 510(k) Premarket Notification Sterile Nitrile Powder Free Examination Gloves Section 5, 510(k) Summary Page 1 of 3 FEB 2 2 2013 #### 510(k) SUMMARY 5. OFFICIAL CORRESPONDENT: DATE: OWNER: September 20, 2012 Northstar Healthcare Holdings 70 Sir John Rogerson's Quay Dublin 2, Ireland Michael Riordan Operations Manager Telephone: 00353-21-4548255 Fax: 00353-21-4548294 Email: michael.riordan@mckesson.ie ## DEVICE NAME: | Trade Name: | Textured Blue Sterile Powder Free Nitrile
Examination Gloves | |--------------------|-----------------------------------------------------------------| | Common Name: | Patient Examination Gloves | | Classification: | Patient Examination Gloves | | Class: | Class I | | Product Code: | LZA | | Regulation Number: | 880.6250 | ## PREDICATE DEVICE(S): | Predicate
510(k) | Device Name | Indication | Clearance
Date | Company | |---------------------|------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------|-----------------------------------| | K081466 | Sterile Nitrile Powder
Free Examination
Gloves | The examination glove is a disposable
device intended for medical and dental
purposes that is worn on the examiner's
hand to prevent contamination between
patient and examiner. | 30 Jul 2008 | Smart Glove
Corp., SDN.
BHD | DEVICE DESCRIPTION: Textured Blue Sterile Powder Free Nitrile Examination Gloves > . . {1}------------------------------------------------ Abbreviated 510(k) Premarket Notification Sterile Nitrile Powder Free Examination Gloves Section 5, 510(k) Summary Page 2 of 3 # STATEMENT OF INTENDED USE: The Textured Blue Sterile Powder Free Nitrile Examination Gloves is a Disposable device intended for medical and dental purposes to be worn on the examiner's hand or finger to prevent contamination between patient and examiner. # TECHNOLOGICAL CHARACTERISTICS: The Textured Blue Sterile Powder Free Nitrile Examination Gloves is substantially equivalent to the predicate device with regard to physical characteristics, design, product features, and intended use. Both gloves are made with nitrile using similar manufacturing processes. | Feature | Sterile Nitrile Powder Free Examination Gloves
K081466
Predicate | Textured Blue Sterile Powder Free Nitrile
Examination Gloves
Proposed | |----------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Intended Use | Intended for medical purposes that is worn on the examiner's hand to
prevent contamination between patient and examiner. | Same | | Indications for
Use Statement | The examination glove is a disposable device intended for medical and
dental purposes that is worn on the examiner's hand to prevent
contamination between patient and examiner. | The examination glove is a disposable device
intended for medical purposes that is worn on the
examiner's hand or finger to prevent
contamination between patient and examiner. | | Description | Sterile, powder free, examination gloves made of nitrile. The gloves are
provided in sizes extra small, small, medium, large and extra large. | Sterile, powder free, examination gloves made of
nitrile. The gloves are provided in sizes small,
medium, and large. | | Presentation | Sterile gloves are provided in dispenser boxes. | Same | | Material | Nitrile | Same | | Sterilization | Sterile | Same | | Single Use | Yes | Same | | Dimensions | Meets ASTM D6319-00a(2005) | Length
Small 230mm min.
Medium 230mm min.
Large 230mm min.
Width
Small 70-90mm
Medium 85-105mm
Large 101-120mm
Thickness Finger 0.08mm min.
Palm 0.06mm min. | | Physical
Properties | Meets ASTM D6319-00a(2005) | Before aging/after aging
Elongation 500% 400%
Tensile Strength 14MPa 14MPa | | Freedom from
Pinholes | Meets ASTM D5151-06 | Same | | Residual
Powder | Meets ASTM D6124-06 | Same | {2}------------------------------------------------ # ASSESSMENT OF NONCLINICAL DATA: | Characteristic | Standard | Device Performance | |-----------------------|--------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------| | Dimension | ASTM Standard
D6319-10 | Meets | | Physical Properties | ASTM Standard
D6319-10 | Meets | | Freedom from Pinholes | 21 CFR 800.20;
ASTM D5151-06 | Meets | | Powder Residual | ASTM Standard
D6124-06 | Meets
Results generated
values below 2mg
of residual
powder | | Biocompatibility | Primary Skin Irritation
in rabbits
(ISO 10993-10:2010)

Dermal Sensitization in
the guinea pig (ISO
10993-10:2010) | Gloves are non-
irritating

Gloves do not
display any
potential for
sensitization | ## CONCLUSIONS: The Textured Blue Sterile Powder Free Nitrile Examination Gloves meet the requirements of established standards ASTM D6319-10, ASTM D5151-06, ASTM D6124-06 and ISO 10993-10:2010. Based on the comparison of intended use, design, materials and performance, the Textured Blue Sterile Powder Free Nitrile Examination Gloves are substantially equivalent to the predicate device. {3}------------------------------------------------ Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three stripes forming its body and wings. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the eagle. #### Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 ### February 22, 2013 Northstar Healthcare Holdings C/O Mr. Ned Devine Responsible Third Party Official Underwriters Laboratories, Incorporated 333 Pfingsten Road NORTHBROOK IL 60062 Re: K122727 Trade/Device Name: Textured Blue Sterile Powder Free Nitrile Examination Gloves Regulation Number: 21 CFR 880.6250 Regulation Name: Patient Examination Glove Regulatory Class: I Product Code: LZA Dated: February 7, 2013 Received: February 8, 2013 ### Dear Mr. Devine: 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. {4}------------------------------------------------ ## Page 2 - Mr. Devine 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 Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related 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 go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH0ffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 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 Small Manufacturers, International and Consumer Assistance 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 yours. Image /page/4/Picture/7 description: The image shows a stylized graphic with illegible text. The text appears to be handwritten and overlaid on top of a geometric design. The design includes a maze-like pattern on the left and a triangular shape on the right, both rendered in black lines. Anthony D. Watson, B.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health ### Enclosure {5}------------------------------------------------ # INDICATIONS FOR USE 510(k) Number (if known): K122727 Textured Blue Sterile Powder Free Nitrile Examination Gloves Device Name: Indications for Use: The examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner. Prescription Use (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use X (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Elizabeî 2013.02 (Division Sign-Off) Division of Anesthesloiogy, General Hospital Infection Control, Dental Devices 510(k) Number;_ Page 1 of 1 ! Northstar Healthcare Holdings --- **Source:** [https://fda-staging.innolitics.com/device/K122727](https://fda-staging.innolitics.com/device/K122727) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com