510(k) K072392 ยท IZL System, X-Ray, Mobile
OPDIMA DIGITAL MAMMOGRAPHIC X-RAY SYSTEM
| Applicant | Siemens Medical Solutions USA, Inc., Mavern PA, US |
| Decision | Substantially Equivalent, Sep 25, 2007 |
| Received | Aug 27, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072392
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.