Physiowave, Inc.
Country not established
- Devices
- 1
What Physiowave, Inc. makes
Physiowave, Inc. manufactures the Cardiovascular Analyzer, a device designed for diagnostic analysis of cardiovascular function and parameters.
The Cardiovascular Analyzer is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Cardiovascular Analzyer Ref K172431
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Physiowave, Inc. have in the registry?
The registry currently lists 1 device for Physiowave, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Physiowave, Inc.'s devices?
Among its 1 most recently registered device, Physiowave, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Physiowave, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Physiowave, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Physiowave, Inc. in the registry?
The most recently registered devices listed for Physiowave, Inc. include Cardiovascular Analzyer.