Prexcor America, Inc.
Country not established
- Devices
- 1
What Prexcor America, Inc. makes
Prexcor America, Inc. manufactures the OASIS CLUB hydromassage device, designed for seated hydrotherapy and muscle relaxation.
The company’s portfolio is regulated under FDA Class II devices, with the OASIS CLUB hydromassage listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Oasis Club Hydromassage Ref K841954
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prexcor America, Inc. have in the registry?
The registry currently lists 1 device for Prexcor America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prexcor America, Inc.'s devices?
Among its 1 most recently registered device, Prexcor America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Prexcor America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Prexcor America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prexcor America, Inc. in the registry?
The most recently registered devices listed for Prexcor America, Inc. include OASIS CLUB HYDROMASSAGE.