510(k) K813139 ยท EAM Screen, Intensifying, Radiographic
KODAK INTENSIFYING SCREEN SO-168
| Applicant | Eastman Kodak Company, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 8, 1981 |
| Received | Nov 6, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813139
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.