Medical Device Manufacturer · US , Clarence , NY

Medisonic U.S.A., Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1989

Total

Cleared

Denied

Medisonic U.S.A., Inc. has 5 FDA 510(k) cleared medical devices. Based in Clarence, US.

Historical record: 5 cleared submissions from 1989 to 1993. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Medisonic U.S.A., Inc.

5 devices

1-5 of 5