Medical Device Manufacturer · CA , St.Laurent, Quebec

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

5 submissions · 5 cleared · Since 2000

Total

Cleared

Denied

Andromed, Inc. has 5 FDA 510(k) cleared medical devices. Based in St.Laurent, Quebec, CA.

Historical record: 5 cleared submissions from 2000 to 2005. Primary specialty: Cardiovascular.

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

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

5 devices

1-5 of 5