Medical Device Manufacturer · US , Waukesha , WI

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

6 submissions · 6 cleared · Since 2008

Total

Cleared

Denied

Prodesse, Inc. has 6 FDA 510(k) cleared medical devices. Based in Waukesha, US.

Historical record: 6 cleared submissions from 2008 to 2009. Primary specialty: Microbiology.

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

Prodesse, Inc. 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 - Prodesse, Inc.

6 devices

1-6 of 6