510(k) K896707 ยท EAM Screen, Intensifying, Radiographic
PERLINK SCREEN, KIRAN SCREEN
| Applicant | Perlink USA, Inc., Rye NY, US |
| Decision | Substantially Equivalent, Aug 30, 1990 |
| Received | Nov 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896707
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.