510(k) K770837 ยท EAM Screen, Intensifying, Radiographic
SCREEN, FINE, LANES, KODAK
| Applicant | Eastman Kodak Company, Mchenry IL, US |
| Decision | Substantially Equivalent, May 26, 1977 |
| Received | May 6, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770837
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.