510(k) K884597 ยท DFH Kappa, Antigen, Antiserum, Control
BECKMAN LAMBDA LIGHT CHAIN REAGENT
| Applicant | Beckman Instruments, Inc., Brea CA, US |
| Decision | Substantially Equivalent, Dec 6, 1988 |
| Received | Oct 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884597
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.