510(k) K103207 ยท OVF Assay, Direct, Nucleic Acid Amplification, Q Fever
JBAIDS Q FEVER DETECTION KIT
| Applicant | Idaho Technology, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, May 20, 2011 |
| Received | Nov 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103207
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.