510(k) K812085 ยท GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2
HERPES VIRUS HOMINIS ANTIBODY TEST SYS.
| Applicant | Zeus Scientific, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 1, 1981 |
| Received | Jul 22, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812085
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.