510(k) K902039 ยท EAM Screen, Intensifying, Radiographic
RAREX & OPTEX X-RAY SCREENS
| Applicant | Mci Optonix, Inc., Cedar Knolls NJ, US |
| Decision | Substantially Equivalent, Jul 27, 1990 |
| Received | May 4, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902039
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.