Medical Device Manufacturer · US , Waukesha , WI

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

10 submissions · 10 cleared · Since 2010

Total

Cleared

Denied

Gen-Probe Prodesse, Inc. has 10 FDA 510(k) cleared microbiology devices. Based in Waukesha, US.

Historical record: 10 cleared submissions from 2010 to 2013.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Gen-Probe 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 - Gen-Probe Prodesse, Inc.

10 devices

1-10 of 10

Cleared Aug 26, 2013

PRODESSE PROFAST+ ASSAY

PRODESSE PROFLU+ ASSAY

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

FDA 510(k) Regulatory Record - Gen-Probe Prodesse, Inc.

Filters