Biofire Diagnostics, Inc. is one of 5184 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biofire Diagnostics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Biofire Diagnostics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 5 cleared submissions from 2013 to 2013. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Biofire Diagnostics, Inc. Filter by specialty or product code using the sidebar.
Biofire Diagnostics, Inc. — FDA 510(k) Products and Clearance History
5 devices
Cleared
Aug 05, 2013
JBAIDS ANTHRAX DETECTION KIT
Microbiology
39d
Cleared
Jul 31, 2013
JBAIDS PLAGUE DETECTION KIT
Microbiology
49d
Cleared
Jul 31, 2013
JBAIDS TULAREMIA DETECTION KIT
Microbiology
34d
Cleared
Jun 21, 2013
FILMARRAY BLOOD CULTURE IDENTIFICATION (BCID) PANEL
Microbiology
80d
Cleared
Feb 11, 2013
FILMARRAY RESPIRATORY PANEL (RP)
Microbiology
80d