Hcg, Inc.
Country not established
- Devices
- 1
What Hcg, Inc. makes
Hcg, Inc. manufactures the Medical Laser Endocoagulator Model P.C., a Class II device designed for endoscopic coagulation procedures.
The device is regulated under FDA’s 510(k) pathway as a Class II medical device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hcg, Inc. have in the registry?
The registry currently lists 1 device for Hcg, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hcg, Inc.'s devices?
Among its 1 most recently registered device, Hcg, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hcg, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hcg, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hcg, Inc. in the registry?
The most recently registered devices listed for Hcg, Inc. include HCG, INC. MEDICAL LASER ENDOCOAGULATOR MODEL P.C..