510(k) K933830 ยท LMA Digitizer, Image, Radiological
KONICA LD-4500 LASER DIGITIZER
| Applicant | Konica Medical Corp., New York NY, US |
| Decision | Substantially Equivalent, Dec 14, 1993 |
| Received | Aug 5, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933830
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.