510(k) K904050 ยท IYX Camera, Scintillation (Gamma)
MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA
| Applicant | Philips Medical Systems (Cleveland), Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Dec 5, 1990 |
| Received | Sep 4, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904050
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.