510(k) K926575 ยท EHD Unit, X-Ray, Extraoral With Timer
MAMMOTEST PRODUCT, MODIFICATION
| Applicant | Fischer Imaging Corp., Denver CO, US |
| Decision | Substantially Equivalent, Mar 30, 1993 |
| Received | Dec 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926575
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.