510(k) K892119 ยท DCK C-Reactive Protein, Antigen, Antiserum, And Control
QUIK-DOT C REACTIVE PROTEIN
| Applicant | Ampcor, Inc., Bridgeport NJ, US |
| Decision | Substantially Equivalent, Apr 14, 1989 |
| Received | Mar 31, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892119
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.