510(k) K100838 ยท IYX Camera, Scintillation (Gamma)
ERGO IMAGING SYSTEM
| Applicant | Digirad Corp., Poway CA, US |
| Decision | Substantially Equivalent, Apr 23, 2010 |
| Received | Mar 24, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100838
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.