510(k) K962019 ยท DCK C-Reactive Protein, Antigen, Antiserum, And Control
C-REACTIVE PROTEIN (CRP):A LATEX SLIDE TEST
| Applicant | Teco Diagnostics, Placentia CA, US |
| Decision | Substantially Equivalent, Nov 25, 1996 |
| Received | May 23, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962019
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.