510(k) K770574 ยท EAM Screen, Intensifying, Radiographic
CRONEX QUANTA III INTENSIFYING SCREENS
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 5, 1977 |
| Received | Mar 28, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770574
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.