510(k) K802590 ยท GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2
DIRECT FLUORESCENT ANTIBODY KIT/HERPES
| Applicant | Bartels & Stout, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Feb 9, 1981 |
| Received | Oct 15, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802590
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.