510(k) K920190 ยท EAM Screen, Intensifying, Radiographic
ULTRA-VISION RAPID INTENSIFYING SCREEN
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, May 28, 1992 |
| Received | Jan 15, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920190
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.