510(k) K160386 ยท MUH System, X-Ray, Extraoral Source, Digital
ReadeR, VieweR, QuickScan PSP
| Applicant | Trident S.R.L, Assago, IT |
| Decision | Substantially Equivalent, Mar 10, 2016 |
| Received | Feb 11, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160386
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.