510(k) K081637 ยท LMC Camera, Multi Format, Radiological
LASER IMAGER DRYPRO MODEL 873
| Applicant | Konica Minolta Medical & Graphic, Inc., New York NY, US |
| Decision | Substantially Equivalent, Jul 1, 2008 |
| Received | Jun 11, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081637
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.