Medical Device Manufacturer · US , Walker , MI

Autovage - FDA 510(k) Cleared Devices

7 submissions · 6 cleared · Since 1982

Total

Cleared

Denied

Autovage has 6 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 6 cleared submissions from 1982 to 1992. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Autovage

7 devices

1-7 of 7