Medical Device Manufacturer · US , Glens Falls , NY

Angiodynamics, Div. E-Z-Em, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1992

Total

Cleared

Denied

Angiodynamics, Div. E-Z-Em, Inc. has 6 FDA 510(k) cleared medical devices. Based in Glens Falls, US.

Historical record: 6 cleared submissions from 1992 to 1996. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Angiodynamics, Div. E-Z-Em, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Angiodynamics, Div. E-Z-Em, Inc.

6 devices

1-6 of 6