(62 days)
No
The document mentions "data and image processing" and "post processed" but does not explicitly mention AI, ML, or related terms like deep learning or neural networks. The description focuses on standard CT technology and features.
No.
The device is used for diagnosis, not therapy. Its output is for "diagnosis of disease, trauma, or abnormality and for planning, guiding and monitoring therapy," implying that the device itself is not therapeutic.
Yes
The Intended Use section explicitly states that the device output is "a valuable medical tool for the diagnosis of disease, trauma, or abnormality." This directly indicates its diagnostic purpose.
No
The device description explicitly lists hardware components such as the gantry, patient table, operator console, and power distribution unit, indicating it is a physical medical device system, not software-only.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the device is an X-ray Computed Tomography system used to produce cross-sectional images of the body. It is used for the diagnosis of disease, trauma, or abnormality and for planning, guiding and monitoring therapy. This involves imaging the inside of the patient's body.
- IVD Definition: In Vitro Diagnostics (IVDs) are medical devices used to perform tests on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections.
- Device Description: The description details a CT scanner system with components like a gantry, patient table, and operator console. These are all components of an imaging system that interacts directly with the patient, not with in vitro samples.
- Input Modality: The input modality is Computed Tomography X-ray, which is an imaging technique applied to the patient.
The device's function is to create images of the body, which is a form of in vivo (within the living body) diagnostic imaging, not in vitro testing.
N/A
Intended Use / Indications for Use
The GE Revolution ACT Computed Tomography X-ray system is intended to produce cross- sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes, for patients of all ages, including Axial, Cine, Helical.
These images may be obtained either with or without contrast. This device may include signal analysis and display equipment, patient, and equipment supports, components and accessories.
This device may include data and image processing to produce images in a variety of trans-axial and reformatted planes. Further the images can be post processed to produce additional imaging planes or analysis results.
The GE Revolution ACT CT Scanner System is indicated for head, whole body and vascular X-ray Computed Tomography applications.
The device output is a valuable medical tool for the diagnosis of disease, trauma, or abnormality and for planning, guiding and monitoring therapy.
Product codes
JAK
Device Description
The multi-slice GE Revolution ACT CT scanner is currently commercially available and in clinical use in various other countries including the EU, Japan, China, and India.
It is a general purpose, 16-slice (detector row) CT scanning system with a z-coverage of 20 mm and a maximum gantry rotation speed of 0.98 seconds. Revolution ACT is designed to help enable greater patient access to CT imaging in facilities that otherwise might not be able to obtain multi-slice CT technology with both current standard and advanced CT features and function.
Revolution ACT uses the same technology, operating principles, features, and functions as the GE Optima CT520 predicate device (K123596) and other cleared GE CT scanners. The system consists of the gantry, patient table, operator console, power distribution unit (PDU), associated accessories, and software options. The Revolution ACT is also available in an 8-detector row (10 mm z-coveragre configuration (Revolution ACTs) using the identical (but depopulated) detector/DAS. The changes from the predicate device do not affect the intended use or patient population.
Becaues the Revolution ACT does not support cardiac or other gated acquisitions, and has a slower rotation time thatn the predicate device, its indications for use were modified by removing cardiac and gated acquisitions and cardiac applications.
Mentions image processing
Yes
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Computed Tomography X-ray
Anatomical Site
head, whole body, vascular
Indicated Patient Age Range
patients of all ages
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Non-Clinical Testing:
Description: Additional engineering bench testing was performed to provide a broad base of system performance testing relevant to demonstrating Revolution ACT's ability for safe and effective diagnostic CT imaging. No new metrics or test methods were needed because of the basic nature (existing technology and features) of Revolution ACT.
Sample Size: Not specified, but involved comparisons using uniform and LCD embedded phantoms.
Key results: Performance testing related to Revolution ACT's ability to scan large patients, performance tests in accordance with IEC 61223-3-5, and testing of the new SmartPlan feature. A comparison of CT number accuracy; CT number uniformity; Image noise (standard deviation); Modulation Transfer Function; Noise Power Spectrum; and Slice thickness between the predicate and subject device was provided. Images from both a uniform phantom and one with embedded LCD objects were provided for the subject device using several reconstruction techniques and a description of the process used to port ASiR onto the new hardware of the subject device.
Clinical Testing:
Description: Sample clinical images reviewed by a board certified radiologist were provided to further verify that the previously cleared iterative reconstruction algorithm worked on the modified hardware platform.
Sample Size: Not specified.
Key results: The device (both 16 and 8-slice configurations) has been in commercial use for clinical diagnosis, and its performance and image quality has been demonstrated to be diagnostically acceptable.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Optima CT520 - K123596
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 892.1750 Computed tomography x-ray system.
(a)
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.(b)
Classification. Class II.
0
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. 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 an eagle, represented by three curved lines that suggest the bird's head, body, and tail feathers.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
GE Hangwei Medical Systems, Co., Ltd. % Wang Xing Regulatory Affairs Manager West Area of Building No.3, No.1 Yongchang North Road Beijing Economic and Technological Development Area 100176 Beijing CHINA
Re: K171013
Trade/Device Name: Revolution ACT Regulation Number: 21 CFR 892.1750 Regulation Name: Computed tomography x-ray system Regulatory Class: II Product Code: JAK Dated: April 5, 2017 Received: April 6, 2017
Dear Wang Xing:
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.
June 5, 2017
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.
Michael D. O'Hara
For
Robert Ochs. Ph.D. Director Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health
Enclosure
2
Image /page/2/Picture/0 description: The image shows the logo for General Electric (GE). The logo is a blue circle with the letters "GE" in a stylized font in the center. The circle has a decorative border with swirling patterns. The logo is simple and recognizable, and it is associated with a well-known company.
GE Healthcare 510(k) Premarket Notification Submission for Revolution ACT
Section 4: Indications for Use Statement
Revolution ACT
3
Indications for Use
510(k) Number (if known) K171013
Device Name Revolution ACT
Indications for Use (Describe)
The GE Revolution ACT Computed Tomography X-ray system is intended to produce cross- sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes, for patients of all ages, including Axial, Cine, Helical.
These images may be obtained either with or without contrast. This device may include signal analysis and display equipment, patient, and equipment supports, components and accessories.
This device may include data and image processing to produce images in a variety of trans-axial and reformatted planes. Further the images can be post processed to produce additional imaging planes or analysis results.
The GE Revolution ACT CT Scanner System is indicated for head, whole body and vascular X-ray Computed Tomography applications.
The device output is a valuable medical tool for the diagnosis of disease, trauma, or abnormality and for planning, guiding and monitoring therapy.
| 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) |
CONTINUE ON A SEPARATE PAGE IF NEEDED.
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 Drug 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."
4
Image /page/4/Picture/0 description: The image shows the logo for General Electric (GE). The logo is a blue circle with the letters "GE" in a stylized script inside. There are small white flourishes around the edge of the circle. The blue color is a medium shade, and the white flourishes add a touch of elegance to the design.
GE Healthcare 510(k) Premarket Notification Submission for Revolution ACT
Section 5: 510(k) Summary
Revolution ACT
5
Image /page/5/Picture/0 description: The image shows the logo for General Electric (GE). The logo is a blue circle with the letters "GE" in a stylized font in the center. There are decorative swirls around the edge of the circle. The logo is simple and recognizable, and it is associated with a well-known company.
510(k) Summary
This 510(k) summary of Safety and Effectiveness information is submitted in accordance with the requirement of 21 CFR Part 807.87(h).
In accordance with 21 CFR 807.92 the following summary of information is provided:
| Date: | March 31, 2017 |
|---|---|
| Submitter: | GE Hangwei Medical System Co.,Ltd |
| West Area of Building No.3, No.1 Yongchang North | |
| Road, Beijing Economic and Technological | |
| Development Area, BEIJING 100176 CHINA | |
| Primary Contact Person: | Wang Xing |
| Regulatory Affairs Manager | |
| GE Healthcare | |
| Phone Number: (86)-10-57388271 | |
| e-mail: xing1.wang@ge.com | |
| Secondary Contact Persons: | John Jaeckle |
| Chief Regulatory Affairs Strategist | |
| GE Healthcare | |
| Phone Number: 262-424-9547 | |
| e-mail: John.Jaeckle.com | |
| Tracey Fox | |
| Regulatory Affairs Director | |
| GE Healthcare | |
| Phone Number: 262-337-2586 | |
| e-mail: tracey.fox@ge.com | |
| Product Identification | Revolution ACT |
| Device Trade Name: | Revolution ACT / Revolution ACTs |
| Common/Usual Name: | Computed Tomography X-ray System |
| Classification Names: | Computed Tomography X-ray System, 21 CFR 892.1750 |
| (Class II) | |
| Product Code: | 90-JAK |
6
Image /page/6/Picture/0 description: The image shows the logo for General Electric (GE). The logo consists of the letters "GE" in a stylized, cursive font, enclosed within a blue circle. Three white, teardrop-shaped elements surround the circle, positioned at the top and sides, adding a decorative touch to the design.
510(k) Premarket Notification Submission for Revolution ACT
| Manufacturer | GE Hangwei Medical System Co.,Ltd
West Area of Building No.3, No.1 Yongchang North
Road, Beijing Economic and Technological
Development Area, BEIJING 100176 CHINA |
|---------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Manufacturing location(s) | GE Hangwei Medical System Co.,Ltd
West Area of Building No.3, No.1 Yongchang North
Road, Beijing Economic and Technological
Development Area, BEIJING 100176 CHINA |
Predicate Device:
Optima CT520 - K123596
Marketed Devices:
The Revolution ACT is a CT device built upon the existing technologies of the predicate device, GE Healthcare' s currently marketed Computed Tomography X-ray System Optima CT520 (K123596). It is of comparable type and substantially equivalent to Optima CT520. In addition, the system has the same intended use and indication for use as that of the predicate device except the cardiac and gated acquisition indications are removed. The system is labeled as the Revolution ACT.
Device Description:
The multi-slice GE Revolution ACT CT scanner is currently commercially available and in clinical use in various other countries including the EU, Japan, China, and India.
It is a general purpose, 16-slice (detector row) CT scanning system with a z-coverage of 20 mm and a maximum gantry rotation speed of 0.98 seconds. Revolution ACT is designed to help enable greater patient access to CT imaging in facilities that otherwise might not be able to obtain multi-slice CT technology with both current standard and advanced CT features and function.
Revolution ACT uses the same technology, operating principles, features, and functions as the GE Optima CT520 predicate device (K123596) and other cleared GE CT scanners. The system consists of the gantry, patient table, operator console, power distribution unit (PDU), associated accessories, and software options. The Revolution ACT is also available in an 8-detector row (10 mm z-coveragre configuration (Revolution ACTs) using the identical (but depopulated) detector/DAS. The changes from the predicate device do not affect the intended use or patient population.
Becaues the Revolution ACT does not support cardiac or other gated acquisitions, and has a slower rotation time thatn the predicate device, its indications for use were modified by removing cardiac and gated acquisitions and cardiac applications.
7
Image /page/7/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'GE' in a stylized, cursive font, enclosed within a blue circle. There are three white swirls around the circle. The logo is simple and recognizable, representing the company's brand identity.
510(k) Premarket Notification Submission for Revolution ACT
Revolution ACT complies with the current IEC 60601-1 Edition 3.1 series of standards (IEC 60601-1-2, 60601-1-3, 60601-2-28, and 60601-2-44), NEMA XR-25, XR-26, and XR-28, and 21 CFR 1020.30 and 1020.33. The materials are the same as those used on other cleared GE CT systems. It has been developed under the GE quality system and has successfully completed design controls activities, including risk management, verification, and validation.
The Revolution ACT is a head and whole body CT system. The device has the same intended use as predicate device Optima CT520 except cardiac and gated acquisition indications are removed. There are no new intended uses for Revolution ACT beyond those of the predicate.
Intended Use:
The GE Revolution ACT CT Scanner System is indicated for head, whole body and vascular X-Ray Computed Tomography applications
Indications for Use:
The GE Revolution ACT Computed Tomography X-ray system is intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes, for patients of all ages, including Axial, Cine, Helical.
These images may be obtained either with or without contrast. This device may include signal analysis and display equipment, patient, and equipment supports, components and accessories.
This device may include data and image processing to produce images in a variety of trans-axial and reformatted planes. Further the images can be post processed to produce additional imaging planes or analysis results.
The GE Revolution ACT CT Scanner System is indicated for head, whole body and vascular X-rav Computed Tomography applications
The device output is a valuable medical tool for the diagnosis of disease, trauma, or abnormality and for planning, quiding and monitoring therapy.
Technology:
The Revolution ACT has a redesigned gantry and new image components. The gantry has a maximum rotation speed of 0.98 seconds, a 65 cm bore, no physical tilt, and a smaller footprint and lower power needs for easier sitina. It incorporates a lower power, single focal spot X-ray tube that is used on other GE systems, and has a redesigned detector that supports a smaller (43 cm) field of view. The detector continues to use GE's
8
Image /page/8/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters "GE" in a stylized script, enclosed within a blue circle. The letters are also blue, matching the color of the circle. The logo is simple and recognizable, representing the brand identity of General Electric.
510(k) Premarket Notification Submission for Revolution ACT
HiLight scintillator. Revolution ACT maintains virtually the same image quality specifications and dose performance as its predicate.
Most the software features and functions are common between the Revolution ACT and its predicate, the others, except for SmartPlan, are available on other cleared GE CT scanners. SmartPlan is designed for workflow enhancement by providing the operator with initial scan set up paraments, such as scan Start and End location, derived from the scout images.
The changes described above do not change the fundamental control mechanism, operating principle, eneray type, and do not change the intended use from the currently commercially available predicate device Optima CT520.
Risk Analysis:
Potential electrical, mechanical, and radiation hazards are identified in risk management including hazard analysis and controlled by:
- System verification and validation to ensure performance to specifications, -Federal Requlations, and user requirements.
- Adherence and certification to industry and international standards. (UL/CSA and -IEC60601-1 Ed.3.1 and associated collateral and particular standards for CT).
- Compliance to applicable CDRH 21CFR subchapter J requirements. -
- Compliance to NEMA XR-25, XR-26, and XR28. -
The device is designed and manufactured under the Quality System Regulations of 21 CFR 820 and ISO 13485.
Determination of Substantial Equivalence:
The Revolution ACT has completed testing and in compliance with AAMI/ANSI ES 60601-1 and IEC60601-1 Ed. 3.1 and its associated collateral and particular standards, 21CFR Subchapter J, and NEMA standards XR25, XR26, and XR28. The device has successfully completed all testing per our quality system as well as addition engineering bench testing in support of this submission. It was designed and is manufactured under the Quality System Regulations of 21CFR 820 and ISO 13485. The following quality assurance measures were applied to the development of the system:
- Risk Analysis
- · Required Reviews
- Design Reviews
- Testing on unit level (Module verification)
- Integration testing (System verification)
- · Performance testing (Verification)
- · Safety testing (Verification)
- Simulated use testing (Validation)
9
Image /page/9/Picture/0 description: The image shows the logo for General Electric (GE). The logo is a blue circle with the letters "GE" in white inside. There are three white teardrop shapes around the circle. The logo is simple and recognizable.
GE Healthcare 510(k) Premarket Notification Submission for Revolution ACT
GE believes the Revolution ACT system is of comparable type and substantially equivalent to our currently marketed system Optima CT520.
The substantial equivalence was also based on software documentation for a "Moderate" level of concern device.
Summary of Additional Testing
Non-Clinical Testing:
In addition to the verification and validation testing successfully completed as required by GE Healthcare's quality system, additional engineering bench testing was performed. The test were chosen to provide a broad base of system performance testing that is relevant to demonstrating Revolution ACT's ability for safe and effective diagnostic CT imaging. Because of the basic nature (existing technology and features) of Revolution ACT, no new metrics or test methods were needed for the bench testing evaluations.
The additional engineering testing performed included performance testing related to Revolution ACT's ability to scan large patients, the performance tests in accordance with IEC 61223-3-5, and testing of the new SmartPlan feature.
A comparision of: CT number accuracy; CT number uniformity; Image noise (standard deviation); Modulation Transfer Function; Noise Power Spectrum; and Slice thickness between the predicate and subject device was provided.
lmages from both a uniform phantom and one with embedded LCD objects were provided for the subject device using several reconstruction techniques.
Additionally provided was a description of the process used to port ASiR onto the new hardware of the subject device.
Clinical Testing:
The type of design changes and having features and functions that are found on the predicate device and other cleared GE CT systems, support using scientific, established, standardized engineering/physics-based verification and performance testing to demonstrate that the device is as safe and as effective as the predicate device.
However, to provide further verification that the previously cleared iterative reconstruction algorithm worked on the modified hardware platform, sample clinical images reviewed by a board certified radiologist were provided.
There are several hundred Revolution ACT systems installed globally. The device (both 16 and 8-slice configurations) have been in commercial use for clinical diagnosis and its performance and image quality has been demonstrated to be diagnostically acceptable.
10
Image /page/10/Picture/0 description: The image shows the General Electric (GE) logo. The logo consists of the letters 'GE' in a stylized, cursive font, enclosed within a blue circle. There are decorative white swirls around the outer edge of the circle, adding a touch of elegance to the design.
510(k) Premarket Notification Submission for Revolution ACT
Substantial Equivalence Conclusion:
Given that:
- . The updated Indications for Use fall within the indicatons for use, and the changes do not represent any new intended uses.
- RevolutionACT has been tested and certified to comply with the above indentifed . standards. And development under our quality system.
- " Verification testing along with additional engineering testing demonstrated Revolution ACT's equivalent performance to currently marketed the predicate and other cleared GE CT devices and is therefore as safe and effective.
- . The changes and the verification, validation, and additional engineering testing did not raise new or different questions of safety and effectiveness, and no new hazards were created.
GE Healthcare believes that the Revolution ACT is as safe and effective for its intended use, and performs in a substantially equivalent manner to the predicate device, Optima CT520