510(k) K933161 ยท EAM Screen, Intensifying, Radiographic
ULTRA-VISION SUPER RAPID INTENSIFYING SCREEN
| Applicant | Dupont Medical Products, Wilmington DE, US |
| Decision | Substantially Equivalent, Oct 7, 1993 |
| Received | Jun 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933161
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.