510(k) K900103 ยท EAM Screen, Intensifying, Radiographic
CRONEX QUANTA SR300 INTENSIFYING SCREEN
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Feb 5, 1990 |
| Received | Jan 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900103
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.