FDA 510(k) Applications for Medical Device Product Code "OEH"
|
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 |