Pro Diagnostics, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Myoglobin Ria Test Kit Ref K915233
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pro Diagnostics, Inc. have in the registry?
The registry currently lists 1 device for Pro Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pro Diagnostics, Inc.'s devices?
Among its 1 most recently registered device, Pro Diagnostics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pro Diagnostics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pro Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pro Diagnostics, Inc. in the registry?
The most recently registered devices listed for Pro Diagnostics, Inc. include MYOGLOBIN RIA TEST KIT.