510(k) K983267 ยท MUH System, X-Ray, Extraoral Source, Digital
DIGORA FOR WINDOWS 2.0
| Applicant | Orion Corporation Soredex, Helsinki, FI |
| Decision | Substantially Equivalent, Dec 30, 1998 |
| Received | Sep 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983267
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.