510(k) K851372 ยท GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2
CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS
| Applicant | Difco Laboratories, Inc., Detroit MI, US |
| Decision | Substantially Equivalent, Jul 12, 1985 |
| Received | Apr 8, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851372
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.