510(k) K061101 ยท GNW Antisera, Cf, Influenza Virus A, B, C
D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT
| Applicant | Diagnostic Hybrids, Inc., Athens OH, US |
| Decision | Substantially Equivalent, Nov 20, 2006 |
| Received | Apr 20, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061101
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.