510(k) K123408 ยท IYX Camera, Scintillation (Gamma)
ERGO IMAGING SYSTEM
| Applicant | Digirad Corp., Poway CA, US |
| Decision | Substantially Equivalent, Jan 15, 2013 |
| Received | Nov 5, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123408
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.