Wildcat Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Wildcat Medical, Inc. makes
Wildcat Medical, Inc. makes the TRIPLEPLAY-VT Vascular Therapy System and the TRIPLEPLAY PRO, which are vascular therapy systems.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Tripleplay-Vt Vascular Therapy System Ref K103187
Regimes: 510(k) Registry: 510(k)Tripleplay Pro Ref K141360
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wildcat Medical, Inc. have in the registry?
The registry currently lists 2 devices for Wildcat Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wildcat Medical, Inc.'s devices?
Among its 2 most recently registered devices, Wildcat Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Wildcat Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Wildcat Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wildcat Medical, Inc. in the registry?
The most recently registered devices listed for Wildcat Medical, Inc. include TRIPLEPLAY-VT VASCULAR THERAPY SYSTEM and TRIPLEPLAY PRO.