Keyamed Na, Inc.
Country not established
- Devices
- 1
What Keyamed Na, Inc. makes
Keyamed Na, Inc. manufactures the DEEPVESSEL FFR, a device used for assessing fractional flow reserve (FFR) in coronary arteries to guide percutaneous coronary intervention (PCI) decisions.
The DEEPVESSEL FFR is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Deepvessel Ffr Ref K213657
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Keyamed Na, Inc. have in the registry?
The registry currently lists 1 device for Keyamed Na, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Keyamed Na, Inc.'s devices?
Among its 1 most recently registered device, Keyamed Na, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Keyamed Na, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Keyamed Na, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Keyamed Na, Inc. in the registry?
The most recently registered devices listed for Keyamed Na, Inc. include DEEPVESSEL FFR.