Medical Device Manufacturer · US , Walker , MI

George W. Cottrell - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1982
1
Total
1
Cleared
0
Denied

George W. Cottrell has 1 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 1 cleared submissions from 1982 to 1982. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by George W. Cottrell Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - George W. Cottrell

1 devices
1-1 of 1
Filters
All1 Neurology 1