510(k) K070206 ยท GQW Antigen, Cf, (Including Cf Control), Varicella-Zoster
DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000
| Applicant | Diagnostic Hybrids, Inc., Athens OH, US |
| Decision | Substantially Equivalent, Aug 30, 2007 |
| Received | Jan 22, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070206
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.