Prism Enterprises, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mityview 4-Way Lateral Expander Speculum Ref K000444
Regimes: 510(k) Registry: 510(k)Mityvac Ref K011532
Regimes: 510(k) Registry: 510(k)Mityvac Merlin, Model 10027 Ref K020447
Regimes: 510(k) Registry: 510(k)Baby Pod Ref K030283
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prism Enterprises, Inc. have in the registry?
The registry currently lists 4 devices for Prism Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prism Enterprises, Inc.'s devices?
Among its 4 most recently registered devices, Prism Enterprises, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Prism Enterprises, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Prism Enterprises, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prism Enterprises, Inc. in the registry?
The most recently registered devices listed for Prism Enterprises, Inc. include MITYVIEW 4-WAY LATERAL EXPANDER SPECULUM, MITYVAC, MITYVAC MERLIN, MODEL 10027 and BABY POD.