510(k) K873167 ยท EAM Screen, Intensifying, Radiographic
KODAK MIN-R MEDIUM SCREEN
| Applicant | Eastman Kodak Company, Rochester NY, US |
| Decision | Substantially Equivalent, Aug 27, 1987 |
| Received | Aug 11, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873167
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.