Promedicon, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ground Aid Caphesive Ref K820405
Regimes: 510(k) Registry: 510(k)Electrosurgical Disp. Dispersive Pad Ref K820196
Regimes: 510(k) Registry: 510(k)Electrosurgical Disp. Dispersive Pad Ref K813434
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promedicon, Inc. have in the registry?
The registry currently lists 3 devices for Promedicon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promedicon, Inc.'s devices?
Among its 3 most recently registered devices, Promedicon, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Promedicon, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Promedicon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promedicon, Inc. in the registry?
The most recently registered devices listed for Promedicon, Inc. include GROUND AID CAPHESIVE and ELECTROSURGICAL DISP. DISPERSIVE PAD.