510(k) K831485 ยท DGC Ige, Antigen, Antiserum, Control
VENTRE/ZYME IGE KIT
| Applicant | Ventrex Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 2, 1983 |
| Received | May 9, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831485
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.