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.

Autovage is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Autovage

7 devices

1-7 of 7