510(k) K792559 ยท GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2
FIAX TEST KIT FOR HERPES SIMPLEX VIRUS
| Applicant | Intl. Diagnostic Technology, Walker MI, US |
| Decision | Substantially Equivalent, Mar 3, 1980 |
| Received | Dec 11, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792559
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.