510(k) K980873 ยท LMA Digitizer, Image, Radiological
KONICA DIRECT DIGITIZER REGIUS MODEL 330
| Applicant | Konica Corp., New York NY, US |
| Decision | Substantially Equivalent, Jun 19, 1998 |
| Received | Mar 6, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980873
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.