Medical Device Manufacturer · US , Rochester , NY

Biosurge, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1987

Total

Cleared

Denied

Biosurge, Inc. has 5 FDA 510(k) cleared medical devices. Based in Rochester, US.

Historical record: 5 cleared submissions from 1987 to 1988. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Biosurge, Inc.

5 devices

1-5 of 5