510(k) K110717 ยท MUE Full Field Digital, System, X-Ray, Mammographic
KONICA MINOLTA XPRESS DIGITAL MAMMOGRAPHY SYSTEM
| Applicant | Konica Minolta Medical & Graphic, Inc., Monroe CT, US |
| Decision | Substantially Equivalent, Dec 23, 2011 |
| Received | Mar 15, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110717
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.