510(k) K110384 ยท IYX Camera, Scintillation (Gamma)
DILON 6800 ACELLA (ACELLA)
| Applicant | Dilon Technologies, Inc., Stillwater MN, US |
| Decision | Substantially Equivalent, May 3, 2011 |
| Received | Feb 10, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110384
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.