510(k) K091171 ยท OMG Antisera, Fluorescent, Human Metapneumovirus
D3 ULTRA DUET DFA RESPIRATORY VIRUS IDENTIFICATION KIT
| Applicant | Diagnostic Hybrids, Inc., Athens OH, US |
| Decision | Substantially Equivalent, Sep 11, 2009 |
| Received | Apr 22, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091171
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.