Gen-Probe, Inc. - FDA 510(k) Cleared Devices
62
Total
62
Cleared
0
Denied
Gen-Probe, Inc. has 62 FDA 510(k) cleared microbiology devices. Based in San Diego, US.
Historical record: 62 cleared submissions from 1985 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.
62 devices
Cleared
Jan 09, 2013
APTIMA TRICHOMONAS VAGINALIS ASSAY - PANTHER
Microbiology
180d
Cleared
May 03, 2012
APTIMA COMBO 2 ASSAY
Microbiology
350d
Cleared
Jan 25, 2007
GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE MODEL#1091
Microbiology
48d
Cleared
Jan 22, 2007
GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS, MODEL 1199
Microbiology
68d
Cleared
Nov 07, 2006
GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE, MODEL 1091
Microbiology
78d
Cleared
Oct 13, 2006
APTIMA CT ASSAY ON THE TIGRIS DTS SYSTEM
Microbiology
144d
Cleared
Oct 04, 2006
TIGRIS DTS GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE, MODEL 1196
Microbiology
125d
Cleared
Aug 17, 2006
TIGRIS DTS GEN-PROBE APTIMA COMBO 2 ASSAY
Microbiology
157d
Cleared
Jul 25, 2006
GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS, MODEL 1088
Microbiology
225d
Cleared
Aug 09, 2005
GEN-PROBE APTIMA COMBO 2 ASSAY
Microbiology
260d
Cleared
Mar 14, 2005
GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE
Microbiology
119d
Cleared
Jan 27, 2005
GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS
Microbiology
80d
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