510(k) K032681 ยท LMC Camera, Multi Format, Radiological
KONICA LASER IMAGER, MODEL DRYPRO MODEL 771
| Applicant | Konica Medical and Graphic Corporation, Mie-Ken, JP |
| Decision | Substantially Equivalent, Sep 24, 2003 |
| Received | Aug 29, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032681
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.