510(k) K101391 ยท IYX Camera, Scintillation (Gamma)
SCANDIA-45 GAMMA CAMERA SYSTEM
| Applicant | Scandia Corporation, Urbandale IA, US |
| Decision | Substantially Equivalent, Aug 4, 2010 |
| Received | May 18, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101391
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.