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.

Grandcor Medical Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Grandcor Medical Systems

8 devices

1-8 of 8