J.A. Gerber Therapeutical, Ltd.
Country not established
- Devices
- 1
What J.A. Gerber Therapeutical, Ltd. makes
J.A. Gerber Therapeutical, Ltd. manufactures the PDB II device, which is classified as a Class I medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
Pdb Ii Ref K830289
510(k) 510(k)
Frequently asked questions
How many devices does J.A. Gerber Therapeutical, Ltd. have in the registry?
The registry currently lists 1 device for J.A. Gerber Therapeutical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list J.A. Gerber Therapeutical, Ltd.'s devices?
Among its 1 most recently registered device, J.A. Gerber Therapeutical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do J.A. Gerber Therapeutical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for J.A. Gerber Therapeutical, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from J.A. Gerber Therapeutical, Ltd. in the registry?
The most recently registered devices listed for J.A. Gerber Therapeutical, Ltd. include PDB II.