510(k) K013052 ยท LMC Camera, Multi Format, Radiological
KONICA LASER IMAGER, DRYPRO MODEL 751/752
| Applicant | Konica Minolta Medical & Graphic, Inc., Hachioji-Shi Tokyo, JP |
| Decision | Substantially Equivalent, Jan 16, 2002 |
| Received | Sep 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013052
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.