510(k) K873529 ยท GQN Antigen, Cf (Including Cf Control), Herpesvirus Hominis 1,2
HYBRIWICK SYSTEM: HERPES DNA PROBE TEST KIT
| Applicant | Diagnostic Hybrids, Inc., Athens OH, US |
| Decision | Substantially Equivalent, Aug 25, 1988 |
| Received | Sep 1, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873529
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.