Datatek, Inc.
Country not established
- Devices
- 1
What Datatek, Inc. makes
Datatek, Inc. makes medical devices such as the PMD SYSTEM-20.
The company's portfolio, which includes Class I devices, is listed in the fda_510k registry and is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pmd System-20 Ref K883390
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Datatek, Inc. have in the registry?
The registry currently lists 1 device for Datatek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Datatek, Inc.'s devices?
Among its 1 most recently registered device, Datatek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Datatek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Datatek, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Datatek, Inc. in the registry?
The most recently registered devices listed for Datatek, Inc. include PMD SYSTEM-20.