American Theracare
Country not established
- Devices
- 1
What American Theracare makes
American Theracare manufactures the Theracare Lounger, a Class I medical device designed for patient positioning and support during therapeutic procedures or recovery.
The device is regulated under FDA 510(k) clearance as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Theracare Lounger Ref K863892
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Theracare have in the registry?
The registry currently lists 1 device for American Theracare. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Theracare's devices?
Among its 1 most recently registered device, American Theracare has devices listed in FDA 510(k) (1 device).
What risk classes do American Theracare's devices fall under?
Among its 1 most recently registered device, the classes recorded for American Theracare's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from American Theracare in the registry?
The most recently registered devices listed for American Theracare include THERACARE LOUNGER.