Medical Device Manufacturer · US , Coon Rapids , MN

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

3 submissions · 3 cleared · Since 1986

Total

Cleared

Denied

Endotronics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Coon Rapids, US.

Historical record: 3 cleared submissions from 1986 to 1988. Primary specialty: Pathology.

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

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

3 devices

1-3 of 3