Medical Device Manufacturer · US , Riviera Beach , FL

Cryodyne Technologies, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1986

Total

Cleared

Denied

Cryodyne Technologies, Inc. has 6 FDA 510(k) cleared medical devices. Based in Riviera Beach, US.

Historical record: 6 cleared submissions from 1986 to 1993. Primary specialty: Pathology.

Browse the FDA 510(k) cleared devices submitted by Cryodyne Technologies, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cryodyne Technologies, Inc.

6 devices

1-6 of 6