510(k) K131936 ยท OEH Joint Biological Agent Identification And Diagnostic System (Jbaids) Tularemia Detection Kit
JBAIDS TULAREMIA DETECTION KIT
| Applicant | Biofire Diagnostics, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jul 31, 2013 |
| Received | Jun 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131936
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.