Medical Device Manufacturer · US , Lowell , MA

Medtronic Andover Medical, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1985

Total

Cleared

Denied

Medtronic Andover Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Lowell, US.

Historical record: 6 cleared submissions from 1985 to 1991. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Medtronic Andover Medical, Inc.

6 devices

1-6 of 6