510(k) K081746 ยท GNW Antisera, Cf, Influenza Virus A, B, C
D3 DUET DFA INFLUENZA A/RESPIRATORY VIRUS SCREENING KIT
| Applicant | Diagnostic Hybrids, Inc., Athens OH, US |
| Decision | Substantially Equivalent, Dec 23, 2008 |
| Received | Jun 19, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081746
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.