Promatek Medical Systems, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Promatron 3000 Ref K901566
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promatek Medical Systems, Inc. have in the registry?
The registry currently lists 1 device for Promatek Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promatek Medical Systems, Inc.'s devices?
Among its 1 most recently registered device, Promatek Medical Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Promatek Medical Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Promatek Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promatek Medical Systems, Inc. in the registry?
The most recently registered devices listed for Promatek Medical Systems, Inc. include PROMATRON 3000.