510(k) K792123 ยท EAM Screen, Intensifying, Radiographic
KODAK LANEX MED. SCREEN
| Applicant | Eastman Kodak Company, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 10, 1979 |
| Received | Oct 25, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792123
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.