Medical Device Manufacturer · US , Mchenry , IL

Gardner Cryogenics - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1977

Total

Cleared

Denied

Gardner Cryogenics has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1977 to 1978. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Gardner Cryogenics

2 devices

1-2 of 2