510(k) K130704 ยท MUE Full Field Digital, System, X-Ray, Mammographic
MICRODOSE SI
| Applicant | Philips Digital Mammography Sweden AB, Solna, SE |
| Decision | Substantially Equivalent, Dec 13, 2013 |
| Received | Mar 15, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130704
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.