510(k) K896059 ยท DCF Albumin, Antigen, Antiserum, Control
MODIFIED QM300 ALBUMIN ANTIBODY PACK
| Applicant | Kallestad Diag, A Div. of Erbamont, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Nov 6, 1989 |
| Received | Oct 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896059
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.