Gynopharma, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Gynopharma, Inc. makes
Gynopharma, Inc. manufactures the medical devices SLIMCATH™ and PROBET™.
These products are classified as Class I and Class II devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Slimcath (Tm) Ref K903001
Regimes: 510(k) Registry: 510(k)Probet (Tm) Ref K903002
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gynopharma, Inc. have in the registry?
The registry currently lists 2 devices for Gynopharma, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gynopharma, Inc.'s devices?
Among its 2 most recently registered devices, Gynopharma, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gynopharma, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gynopharma, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gynopharma, Inc. in the registry?
The most recently registered devices listed for Gynopharma, Inc. include SLIMCATH (TM) and PROBET (TM).