510(k) K860755 ยท EAM Screen, Intensifying, Radiographic
KODAK MIN-R FAST SCREEN SO-459
| Applicant | Eastman Kodak Company, Rochester NY, US |
| Decision | Substantially Equivalent, Mar 6, 1986 |
| Received | Feb 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860755
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.