Anoxia Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Anoxia Medical, Inc. makes
Anoxia Medical, Inc. makes the Slinky Catheter and Quiver Aspiration Pump.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Slinky Catheter Ref K231179
Regimes: 510(k) Registry: 510(k)Quiver Aspiration Pump Ref K232831
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anoxia Medical, Inc. have in the registry?
The registry currently lists 2 devices for Anoxia Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anoxia Medical, Inc.'s devices?
Among its 2 most recently registered devices, Anoxia Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Anoxia Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Anoxia Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anoxia Medical, Inc. in the registry?
The most recently registered devices listed for Anoxia Medical, Inc. include Slinky Catheter and Quiver Aspiration Pump.