Gary A. Gelbfish
Country not established
- Devices
- 1
What Gary A. Gelbfish makes
Gary A. Gelbfish manufactures the GELBFISH ENDO-VAC SYSTEM, a medical device designed for endoscopic vacuum-assisted procedures, likely used in minimally invasive surgical applications.
The device is classified as Class II under FDA regulations and is listed in the FDA 510(k) registry. The manufacturer is based in the United States.
Catalogue
Gelbfish Endo-Vac System Ref K970233
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gary A. Gelbfish have in the registry?
The registry currently lists 1 device for Gary A. Gelbfish. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gary A. Gelbfish's devices?
Among its 1 most recently registered device, Gary A. Gelbfish has devices listed in FDA 510(k) (1 device).
What risk classes do Gary A. Gelbfish's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gary A. Gelbfish's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gary A. Gelbfish in the registry?
The most recently registered devices listed for Gary A. Gelbfish include GELBFISH ENDO-VAC SYSTEM.