Physion, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Miniphysionizer 2.0 And Electrodes Ref K022950
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Physion, Inc. have in the registry?
The registry currently lists 2 devices for Physion, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Physion, Inc.'s devices?
Among its 2 most recently registered devices, Physion, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Physion, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Physion, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Physion, Inc. in the registry?
The most recently registered devices listed for Physion, Inc. include MINIPHYSIONIZER 2.0 AND ELECTRODES and N-DO ENDOINJECTOR NEEDLE, MODEL PH00961109 AND PH00961110.