510(k) K911345 ยท GQN Antigen, Cf (Including Cf Control), Herpesvirus Hominis 1,2
HSV IN SITU DNA PROBE HYBRIDIZATION TEST KIT
| Applicant | Diagnostic Hybrids, Inc., Athens OH, US |
| Decision | Substantially Equivalent, Jun 17, 1991 |
| Received | Mar 27, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911345
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.