Enhanced Perfusion Systems, Inc.
Country not established
- Devices
- 1
What Enhanced Perfusion Systems, Inc. makes
Enhanced Perfusion Systems, Inc. manufactures the GENTLE HEADER, a device designed for controlled fluid management in perfusion applications, ensuring gentle and regulated flow during medical procedures.
The GENTLE HEADER is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Gentle Header Ref K902845
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Enhanced Perfusion Systems, Inc. have in the registry?
The registry currently lists 1 device for Enhanced Perfusion Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Enhanced Perfusion Systems, Inc.'s devices?
Among its 1 most recently registered device, Enhanced Perfusion Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Enhanced Perfusion Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Enhanced Perfusion Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Enhanced Perfusion Systems, Inc. in the registry?
The most recently registered devices listed for Enhanced Perfusion Systems, Inc. include GENTLE HEADER.