510(k) K963913 ยท EAM Screen, Intensifying, Radiographic
MD100 & MM150
| Applicant | Konica Medical Corp., New York NY, US |
| Decision | Substantially Equivalent, Oct 8, 1997 |
| Received | Sep 30, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963913
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.