510(k) K930501 ยท JIS Calibrator, Primary
DU PONT ACA NEV/EEV VERIFIER
| Applicant | Dupont Medical Products, Wilmington DE, US |
| Decision | Substantially Equivalent, Aug 9, 1993 |
| Received | Feb 1, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930501
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.