510(k) K081829 ยท IYX Camera, Scintillation (Gamma)
CAPIMAGE
| Applicant | Danish Diagnostic Development A/S, Horsholm, DK |
| Decision | Substantially Equivalent, Jul 11, 2008 |
| Received | Jun 27, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081829
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.