510(k) K012170 ยท MUH System, X-Ray, Extraoral Source, Digital
DIGORA PCT
| Applicant | Soredex Palodex Group OY, Helsinki, FI |
| Decision | Substantially Equivalent, Aug 10, 2001 |
| Received | Jul 12, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012170
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.