Medical Device Manufacturer · US , Brooklyn , NY

Dresser Argus, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

Dresser Argus, Inc. has 2 FDA 510(k) cleared medical devices. Based in Brooklyn, US.

Historical record: 2 cleared submissions from 1988 to 1991. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Dresser Argus, Inc.

2 devices

1-2 of 2