510(k) K934949 ยท IXK System, Imaging, X-Ray, Electrostatic
DIGORA
| Applicant | Orion Corporation Soredex, Helsinki, FI |
| Decision | Substantially Equivalent, Feb 10, 1994 |
| Received | Oct 18, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934949
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.