510(k) K904167 ยท GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2
PATHODX HERPES TYPING
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Dec 13, 1990 |
| Received | Sep 11, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904167
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.