SYNGO CT 2014A (SOMARIS/5 VB42) FOR SOMATOM EMOTION & SENSATION FAMILY CT
Device Facts
| Record ID | K140232 |
|---|---|
| Device Name | SYNGO CT 2014A (SOMARIS/5 VB42) FOR SOMATOM EMOTION & SENSATION FAMILY CT |
| Applicant | Siemens Medical Solutions USA, Inc. |
| Product Code | JAK · Radiology |
| Decision Date | Aug 14, 2014 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 892.1750 |
| Device Class | Class 2 |
Indications for Use
The SOMATOM Emotion and SOMATOM Sensation family CT systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes* taken at different angles. (*spiral planes: the axial planes resulted from the continuous rotation of detectors and x-ray tube, and the simultaneous translation of the patient.)
Device Story
syngo® CT 2014A (SOMARIS/5 VB42) is a software upgrade for existing SOMATOM Emotion and Sensation CT systems. The software manages patient data, controls X-ray scanning, performs image reconstruction, and handles image archiving/evaluation. It processes X-ray transmission data acquired via rotating detectors and X-ray tubes to generate cross-sectional DICOM images. Operated by clinicians in a hospital or clinic setting, the software provides tools for dose management (Dose MAP), scan initiation (e-Start), and iterative reconstruction (IRIS). The output consists of diagnostic CT images used by radiologists and physicians to inform clinical decision-making and patient diagnosis. The upgrade includes bug fixes and feature parity with other commercially available Siemens CT systems.
Clinical Evidence
Bench testing only. Verification and validation testing, including phantom testing, were conducted to confirm software performance and adherence to specifications. Risk management and hazard analysis were performed in accordance with ISO 14971. No clinical data was required or provided.
Technological Characteristics
Software-based command program for CT systems. Operates on existing hardware (tube, collimator, detector, DAS). Connectivity via DICOM. Complies with IEC 62304 (software lifecycle), ISO 14971 (risk management), IEC 60601-1 (safety), and NEMA XR-25 (Dose Check). Features include Dose MAP, e-Start, and IRIS iterative reconstruction.
Indications for Use
Indicated for whole-body X-ray computed tomography imaging in patients requiring cross-sectional diagnostic visualization.
Regulatory Classification
Identification
A computed tomography x-ray system is a diagnostic x-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from the same axial plane taken at different angles. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.
Predicate Devices
- syngo® CT 2013A (SOMARIS/5 VC20B) (K133424)
- SOMATOM Project P30F/ Sensation 64 (K040655)
- SOMATOM Project P30L/ Sensation Open (K040577)
- SOMATOM P30 CT Systems/ Sensation (K013522)
Submission Summary (Full Text)
{0}------------------------------------------------
Image /page/0/Picture/1 description: The image is a seal for the Department of Health & Human Services - USA. The seal is circular and contains the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. In the center of the seal is an abstract symbol that resembles a stylized caduceus, with three human profiles facing to the right.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
August 14, 2014
Siemens Medical Solutions, USA, Inc. % Ms. Eve Davis Regulatory Affairs Specialist 51 Valley Stream Parkway D02 MALVERN PA 19355
Re: K140232
Trade/Device Name: syngo® CT 2014A (SOMARIS/5 VB42) for SOMATOM Emotion & SOMATOM Sensation family CT systems Regulation Number: 21 CFR 892.1750 Regulation Name: Computed tomography x-ray system Regulatory Class: II Product Code: JAK Dated: August 15, 2014 Received: July 6, 2014
Dear Ms. Davis:
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 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.
{1}------------------------------------------------
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/Resourcesfor You/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 yours.
Sm. 7)
for
Janine M. Morris Director Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health
Enclosure
{2}------------------------------------------------
# Indications for Use
510(k) Number (if known) K140232
Device Name
syngo® CT 2014A (SOMARIS/5 VB42) for SOMATOM Emotion & SOMATOM Sensation family CT systems
Indications for Use (Describe)
The SOMATOM Emotion and SOMATOM Sensation family CT systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes" taken at different angles.
(*spiral planes: the axial planes resulted from the continuous rotation of detectors and x-ray tube, and the simultaneous translation of the patient.)
Type of Use (Select one or both, as applicable)
> Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
## PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED.
## FOR FDA USE ONLY
Concurrence of Center for Devices and Radiological Health (CDRH) (Signature)
This section applies only to requirements of the Paperwork Reduction Act of 1995.
## *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
> Department of Health and Human Services Food and Druq Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
{3}------------------------------------------------
Image /page/3/Picture/0 description: The image shows the word "SIEMENS" in a sans-serif font. The letters are a light blue color, and there is a black line underneath the word. The word is in all capital letters and is centered in the image.
(SOMARIS/5 VB42) for SOMATOM Emotion & Sensation family CT systems
510(k) Summary
Submitted by: Siemens Medical Solutions USA, Inc. 51 Valley Stream Parkway Malvern, PA 19355
Date Prepared: July 15, 2014
This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR §807.92.
- 1. General Information Importer/Distributor: Siemens Medical Solutions USA, Inc. 51 Valley Stream Parkway Malvern, PA 19355
Establishment Reqistration Number: 2240869
Manufacturing Site: SIEMENS SHANGHAI, MEDICAL EQUIPMENT LTD. 278 Zhou Zhu Rd Shanghai, CHINA 201318
Establishment Registration Number: 3003202425
- 2. Contact Person:
Eve Davis Regulatory Affairs Specialist, Regulatory Affairs Submissions Siemens Medical Solutions, Inc. USA 51 Valley Stream Parkway D02 Malvern, PA 19355-1406 Phone: (610) 219-7133 Fax: (610) 448-1778 Email: eve.davis@siemens.com
#### 3. Device Name and Classification
| Product Name: | syngo® CT 2014A (SOMARIS/5 VB42) for SOMATOM Emotion & SOMATOM Sensation family CT systems |
|-----------------------|--------------------------------------------------------------------------------------------|
| Propriety Trade Name: | syngo® CT 2014A (SOMARIS/5 VB42) for SOMATOM Emotion & SOMATOM Sensation family CT systems |
| Classification Name: | Computed Tomography X-ray System |
| Classification Panel: | Radiology |
| CFR Section: | 21 CFR §892.1750 |
| Device Class: | Class II |
| Product Code: | JAK |
{4}------------------------------------------------
### Substantial Equivalence: 4.
Siemens syngo® CT 2014A (SOMARIS/5 VB42) for SOMATOM Emotion & SOMATOM Sensation family CT systems is substantially equivalent to the following medical devices in commercial distribution:
| Predicate Devices | FDA Clearance<br>Number | FDA Clearance<br>Date |
|--------------------------------------|-------------------------|-----------------------|
| syngo® CT 2013A (SOMARIS/5 VC20B) | K133424 | January 17, 2014 |
| SOMATOM Project P30F/ Sensation 64 | K040655 | April 2, 2004 |
| SOMATOM Project P30L/ Sensation Open | K040577 | March 22, 2004 |
| SOMATOM P30 CT Systems/ Sensation | K013522 | November 07, 2001 |
#### 5. Device Description:
syngo® CT 2014A (SOMARIS/5 VB42) is a new scanning software version for the following, already commercially available, systems:
- SOMATOM Emotion 6 CT System ●
- SOMATOM Emotion 16 ●
- SOMATOM Project P30F/Sensation 64 ●
- SOMATOM Project P30L/Sensation Open ●
- SOMATOM P30 CT/Sensation .
The system software is a command-based program used for patient management, data management, X-ray scan control, image reconstruction, and image archive/evaluation. This new software version, syngo® CT 2014A (SOMATOM Emotion & SOMARIS/5 VB42), supports bug fixing and an upgrade for the existing commercially available SOMATOM Sensation family CT systems for better maintenance.
The SOMATOM Emotion and SOMATOM Sensation family CT systems are whole body X-ray Computed Tomography Systems. They produce CT images in DICOM format, which can be used by post-processing applications commercially distributed by Siemens and other vendors.
### 6. Summary of Technical Characteristics of the Subject Device as Compared with the Predicate Device:
There are no significant changes in the materials, energy source, or technological characteristics when compared to the predicate devices for syngo® CT 2014A (SOMARIS/5 VB42) for SOMATOM Emotion & SOMATOM Sensation family CT systems. The imaging components (tube, collimator, detector, and DAS) are the same as the predicate devices.
In addition to the bug fixing and upgrade, the new software version syngo® CT 2014A (SOMARIS/5 VB42) supports features which already exist on other commercially available SOMATOM Emotion and SOMATOM Sensation Family CT
{5}------------------------------------------------
Image /page/5/Picture/0 description: The image shows the word "SIEMENS" in a sans-serif font. The letters are a light blue color. There is a black line underneath the word.
(SOMARIS/5 VB42) for SOMATOM Emotion & Sensation family CT systems
Systems. These features are now also provided to the above mentioned systems, which have been installed or were in use prior to their introduction. These features are:
- Dose MAP ●
- . e-Start Functionality
- . IRIS
#### Nonclinical Testing: 7.
The SOMATOM Emotion and SOMATOM Sensation family CT systems configured with software version syngo® CT 2014A (SOMARİS/5 VB42) are designed to fulfill the requirements of the following standards:
| Recognition<br>Number | Product<br>Area | Title of Standard | Reference<br>Number &<br>Date | Publication<br>Date | Standards<br>Development<br>Organization |
|-----------------------|-----------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------|---------------------|------------------------------------------|
| 5-40 | General | Medical devices –<br>Application of risk<br>management to medical<br>devices | 14971<br>Second<br>Edition 2007-<br>03-01 | 08/20/2012 | ISO |
| 13-8 | Software | Medical device software –<br>Software life cycle processes | 62304 First<br>edition 2006-<br>05 | 08/20/2012 | IEC |
| 5-41 | General | Medical electrical equipment<br>– Part 1-4: General<br>requirements for safety –<br>Collateral standard:<br>Programmable electrical<br>medical systems, edition 1.1 | 60601-1-4:<br>2000<br>Consol.Ed<br>1.1 | 09/08/2009 | IEC |
| 12-218 | Radiology | Digital Imaging and<br>Communications in Medicine<br>(DICOM) Set | PS 3.1-3.15,<br>2001 | 3/18/2011 | NEMA |
| 12-222 | Radiology | Evaluation and routine<br>testing in medical imaging<br>departments - Part 3-5:<br>Acceptance tests - Imaging<br>performance of computed<br>tomography X-ray equipment | 61223-3-5<br>First edition<br>2004-08 | 03/18/2011 | IEC |
| 12-226 | Radiology | Evaluation and routine<br>testing in medical imaging<br>departments - Part 2-6:<br>Constancy tests - Imaging<br>performance of computed | 61223-2-6<br>Second<br>Edition 2006-<br>11 | 02/28/2011 | IEC |
{6}------------------------------------------------
| | | tomography X-ray equipment | | | |
|--------|-----------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------|------------|------------------|
| 12-225 | Radiology | Computed Tomography<br>Dose Check | XR-25 | 03/18/2011 | NEMA |
| 5-78 | General | A2:2010/(R)2012<br>(Consolidated Text) Medical<br>electrical equipment-Part 1:<br>General requirements for<br>basic safety and essential<br>performance (IEC 60601-<br>1:2005, MOD) | ES60601-<br>1:2005/(R)20<br>12 and<br>C1:2009/(R)<br>2012 and<br>a2:2010/(R)2<br>012 | 01/14/2014 | AAMI ANSI |
| 5-53 | General | Medical electrical equipment-<br>Part 1-2: General<br>requirements for basic safety<br>and essential performance-<br>Collateral standard:<br>Electromagnetic<br>compatibility-Requirements<br>and tests | 60601-1-2<br>Edition<br>3:2007-03 | 01/30/2014 | IEC |
| 5-54 | General | Medical electrical equipment-<br>Part 1-2: General<br>requirements for basic safety<br>and essential performance-<br>Collateral standard:<br>Electromagnetic<br>compatibility-Requirements<br>and tests (Edition 3) | 60601-1-<br>2:2007/(R)20<br>12 | 01/30/2014 | AAMI ANSI<br>IEC |
| 12-257 | Radiology | Medical electrical equipment-<br>Part 2-44: Particular<br>requirements for the basic<br>safety and essential<br>performance of X-ray<br>equipment for X-ray<br>equipment for computed<br>tomography | 60601-2-44<br>Edition 3.0<br>2009-02 | 01/14/2014 | IEC |
Non-clinical tests were conducted for the SOMATOM Emotion & SOMATOM Sensation family CT systems configured with software version syngo® CT 2014A (SOMARIS/5 VB42) during product development. The modifications described in this Premarket Notification were supported with verification/validation as well as phantom testing.
The Risk analysis was completed and risk control implemented to mitigate identified hazards. The testing results support the conclusion that all of the software specifications have met the acceptance criteria. Testing for verification and validation of the device was found acceptable to support the claims of substantial equivalence.
FDA's Guidance Document "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices" issued on May 11, 2005, was adhered to.
{7}------------------------------------------------
## (SOMARIS/5 VB42) for SOMATOM Emotion & Sensation family CT systems
#### 8. Indications for Use:
The SOMATOM Emotion and SOMATOM Sensation family CT systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes* taken at different angles.
(*spiral planes: the axial planes resulted from the continuous rotation of detectors and x-ray tube, and the simultaneous translation of the patient.)
#### 9. General Safety and Effectiveness Concerns:
The device labeling contains instructions for use as well as necessary cautions and warnings to provide for safe and effective use of the device.
Risk management is ensured via a hazard analysis. Potential hazards are controlled during development, verification and validation testing. To minimize electrical, mechanical, and radiation hazards, Siemens adheres to recognized and established industry practice and standards.
#### 10. Conclusion as to Substantial Equivalence
In summary, Siemens is of the opinion that syngo® CT 2014A (SOMARIS/5 VB42) for SOMATOM Emotion & SOMATOM Sensation family CT systems does not introduce any new potential safety risk, and is substantially equivalent to and performs as well as the predicate devices.
