Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Biofire Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K131930 JBAIDS ANTHRAX DETECTION KITNHT2013-08-05 View
510(k) K131729 JBAIDS PLAGUE DETECTION KITOIH2013-07-31 View
510(k) K131936 JBAIDS TULAREMIA DETECTION KITOEH2013-07-31 View
510(k) K130914 FILMARRAY BLOOD CULTURE IDENTIFICATION (BCID) PANELPEN2013-06-21 View
510(k) K123620 FILMARRAY RESPIRATORY PANEL (RP)OCC2013-02-11 View
↑