510(k) K922483 ยท KPX Changer, Radiographic Film/Cassette
DU PONT COMPACT DAYLIGHT SYSTEM 2000
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Sep 11, 1992 |
| Received | May 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922483
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.