Gen-Probe Prodesse, Inc. is one of 5178 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gen-Probe Prodesse, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
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. — FDA 510(k) Products and Clearance History
10 devices
Cleared
Aug 26, 2013
PRODESSE PROFAST+ ASSAY
Microbiology
39d
Cleared
Aug 26, 2013
PROPARAFLU+ ASSAY
Microbiology
39d
Cleared
Aug 14, 2013
PROADENO+ ASSAY
Microbiology
33d
Cleared
Aug 14, 2013
PRO HMPV+ ASSAY
Microbiology
29d
Cleared
Aug 09, 2013
PRODESSE PROFLU+ ASSAY
Microbiology
30d
Cleared
Jan 16, 2013
PROGASTRO SSCS ASSAY
Microbiology
89d
Cleared
Jan 16, 2013
PRO HMPV+ ASSAY
Microbiology
34d
Cleared
Jun 27, 2011
PROFLU+ ASSAY
Microbiology
82d
Cleared
Dec 03, 2010
PRODESSE PROADENO
Microbiology
59d
Cleared
Jul 23, 2010
PROFAST+ ASSAY
Microbiology
22d