510(k) K882998 ยท DCK C-Reactive Protein, Antigen, Antiserum, And Control
ACUTE PHASE C-REACTIVE PROTEIN LATEX AGGLU. TEST
| Applicant | Amtec Diagnostics International, Inc., Conroe TX, US |
| Decision | Substantially Equivalent, Sep 7, 1988 |
| Received | Jul 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882998
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.