510(k) K942399 ยท EAM Screen, Intensifying, Radiographic
KYOKKO UM SERIES INTENSIFYING SCREEN
| Applicant | Fujifilm Medical System U.S.A., Inc., Stamford CT, US |
| Decision | Substantially Equivalent, Jun 10, 1994 |
| Received | May 19, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942399
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.