FDA 510(k) Applications for Medical Device Product Code "OEH"
(Joint Biological Agent Identification And Diagnostic System (Jbaids) Tularemia Detection Kit)

FDA 510(k) Number Applicant Device Name Decision Date
K131936 BIOFIRE DIAGNOSTICS, INC. JBAIDS TULAREMIA DETECTION KIT 07/31/2013
K072547 IDAHO TECHNOLOGY, INC. JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124 12/19/2007


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