510(k) K860033 ยท DGC Ige, Antigen, Antiserum, Control
EIA MONOCLONAL TOTAL IGE KIT
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Apr 7, 1986 |
| Received | Jan 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860033
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.