Centaur Sciences, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Centaur Sciences, Inc. makes
Centaur Sciences, Inc. makes the Guardian II I.V. Controller and the CentaurSet 300 & 300 P.E.D.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Guardian Ii I.V. Controller Ref K790836
Regimes: 510(k) Registry: 510(k)Centaurset 300 & 300 P.E.D Ref K830258
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Centaur Sciences, Inc. have in the registry?
The registry currently lists 2 devices for Centaur Sciences, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Centaur Sciences, Inc.'s devices?
Among its 2 most recently registered devices, Centaur Sciences, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Centaur Sciences, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Centaur Sciences, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Centaur Sciences, Inc. in the registry?
The most recently registered devices listed for Centaur Sciences, Inc. include GUARDIAN II I.V. CONTROLLER and CENTAURSET 300 & 300 P.E.D.