510(k) K896739 ยท LMA Digitizer, Image, Radiological
KONICA KFDR-S
| Applicant | Konica Medical Corp., New York NY, US |
| Decision | Substantially Equivalent, Apr 30, 1990 |
| Received | Nov 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896739
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.