Promedica, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
The Ultra System Sp Ref K032813
Regimes: 510(k) Registry: 510(k)The Ultra System Ref K032445
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promedica, Inc. have in the registry?
The registry currently lists 2 devices for Promedica, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promedica, Inc.'s devices?
Among its 2 most recently registered devices, Promedica, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Promedica, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Promedica, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promedica, Inc. in the registry?
The most recently registered devices listed for Promedica, Inc. include THE ULTRA SYSTEM SP and THE ULTRA SYSTEM.