Medical Device Manufacturer · US , Beaverton , OR

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

7 submissions · 7 cleared · Since 1989

Total

Cleared

Denied

Vidco, Inc. has 7 FDA 510(k) cleared medical devices. Based in Beaverton, US.

Historical record: 7 cleared submissions from 1989 to 1997. Primary specialty: Cardiovascular.

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

Vidco, Inc. is one of 12331 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

7 devices

1-7 of 7