510(k) K992586 ยท LMC Camera, Multi Format, Radiological
KONICA LASER IMAGER, DRYPRO MODEL 722
| Applicant | Konica Corp., Mie-Ken, JP |
| Decision | Substantially Equivalent, Oct 29, 1999 |
| Received | Aug 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992586
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.