Imedrix Inc. (Formerly Piitech Inc.)
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
KardioScreen Ref K191692
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Imedrix Inc. (Formerly Piitech Inc.) have in the registry?
The registry currently lists 1 device for Imedrix Inc. (Formerly Piitech Inc.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Imedrix Inc. (Formerly Piitech Inc.)'s devices?
Among its 1 most recently registered device, Imedrix Inc. (Formerly Piitech Inc.) has devices listed in FDA 510(k) (1 device).
What risk classes do Imedrix Inc. (Formerly Piitech Inc.)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Imedrix Inc. (Formerly Piitech Inc.)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Imedrix Inc. (Formerly Piitech Inc.) in the registry?
The most recently registered devices listed for Imedrix Inc. (Formerly Piitech Inc.) include KardioScreen.