510(k) K891782 ยท GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2
HSV-2 ELISA TEST SYSTEM
| Applicant | Zeus Scientific, Inc., Raritan NJ, US |
| Decision | Substantially Equivalent, Jun 20, 1989 |
| Received | Mar 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891782
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.