Physio-Dyne
Country not established
- Devices
- 1
What Physio-Dyne makes
Physio-Dyne makes the Physio-Dyne Easi-Lab device.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Physio-Dyne Easi - Lab Ref K922660
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Physio-Dyne have in the registry?
The registry currently lists 1 device for Physio-Dyne. Devices recorded under merged duplicate company entries are counted once.
Which registries list Physio-Dyne's devices?
Among its 1 most recently registered device, Physio-Dyne has devices listed in FDA 510(k) (1 device).
What risk classes do Physio-Dyne's devices fall under?
Among its 1 most recently registered device, the classes recorded for Physio-Dyne's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Physio-Dyne in the registry?
The most recently registered devices listed for Physio-Dyne include PHYSIO-DYNE EASI - LAB.