510(k) K884745 ยท DLJ Calibrators, Drug Specific
DU PONT ACA METHOTREXATE CALIBRATOR
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Jan 30, 1989 |
| Received | Nov 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884745
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.