510(k) K974423 ยท EAM Screen, Intensifying, Radiographic
ULTRA-VISION MAMMOGRAPHY DETAIL, ULTRA-VISION MAMMOGRAPHY FAST DETAIL
| Applicant | Sterling Diagnostic Imaging, Inc., Greenville SC, US |
| Decision | Substantially Equivalent, Dec 22, 1997 |
| Received | Nov 24, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974423
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.