510(k) K875165 ยท DEH Lambda, Antigen, Antiserum, Control
QM300 LAMBDA LIGHT CHAINS ANTIBODY PACK
| Applicant | Kallestad Diag, A Div. of Erbamont, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Jan 22, 1988 |
| Received | Dec 16, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875165
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.