Medical Device Manufacturer · US , Dayton , OH

Grandcor Medical Systems - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1986

Total

Cleared

Denied

Grandcor Medical Systems has 8 FDA 510(k) cleared medical devices. Based in Dayton, US.

Historical record: 8 cleared submissions from 1986 to 1991. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Grandcor Medical Systems Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Grandcor Medical Systems

8 devices

1-8 of 8