Medical Device Manufacturer · MC , Monaco

Promepla Sam - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2012

Total

Cleared

Denied

Promepla Sam has 5 FDA 510(k) cleared medical devices. Based in Monaco, MC.

Historical record: 5 cleared submissions from 2012 to 2018. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Promepla Sam

5 devices

1-5 of 5