510(k) K920558 ยท KPR System, X-Ray, Stationary
KONICA DIRECT DIGITIZER KD-1000
| Applicant | Konica Corp., New York NY, US |
| Decision | Substantially Equivalent, Mar 6, 1992 |
| Received | Dec 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920558
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.