Medical Device Manufacturer · US , Princeton , NJ

Gynopharma, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991

Total

Cleared

Denied

Gynopharma, Inc. has 2 FDA 510(k) cleared medical devices. Based in Princeton, US.

Historical record: 2 cleared submissions from 1991 to 1991. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Gynopharma, Inc. Filter by specialty or product code using the sidebar.

2 devices

1–2 of 2

Data Source

FDA 510(k) public files . 174,402 total devices indexed.