510(k) K890530 ยท DGC Ige, Antigen, Antiserum, Control
N LATEX IGE KIT (IMMUNOGLOBULIN E REAGENTS)
| Applicant | Behring Diagnostics, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Mar 27, 1989 |
| Received | Feb 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890530
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.