Medical Device Manufacturer · US , White Plains , NY

Combe Incorporated - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2014

Total

Cleared

Denied

Combe Incorporated has 3 FDA 510(k) cleared medical devices. Based in White Plains, US.

Historical record: 3 cleared submissions from 2014 to 2017. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Combe Incorporated Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Combe Incorporated

3 devices

1-3 of 3