Golden Gate Bio-Device
Country not established
- Devices
- 1
What Golden Gate Bio-Device makes
Golden Gate Bio-Device manufactures the PALJET-B device, which is classified as a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Paljet-B Ref K973663
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Golden Gate Bio-Device have in the registry?
The registry currently lists 1 device for Golden Gate Bio-Device. Devices recorded under merged duplicate company entries are counted once.
Which registries list Golden Gate Bio-Device's devices?
Among its 1 most recently registered device, Golden Gate Bio-Device has devices listed in FDA 510(k) (1 device).
What risk classes do Golden Gate Bio-Device's devices fall under?
Among its 1 most recently registered device, the classes recorded for Golden Gate Bio-Device's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Golden Gate Bio-Device in the registry?
The most recently registered devices listed for Golden Gate Bio-Device include PALJET-B.