510(k) K862414 ยท EAM Screen, Intensifying, Radiographic
FUJI CR IMAGING PLATE
| Applicant | Parexel Intl. Corp., Cambridge MA, US |
| Decision | Substantially Equivalent, Feb 26, 1987 |
| Received | Jun 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862414
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.