510(k) K880341 ยท DFH Kappa, Antigen, Antiserum, Control
N-IMMUNOGLOBULIN LIGHT CHAIN KIT
| Applicant | Behring Diagnostics, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Feb 17, 1988 |
| Received | Jan 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880341
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.