510(k) K950317 ยท IXL Device, Spot-Film
ADVANTX 1824 SPOTFILM DEVICE
| Applicant | GE Medical Systems, Waukesha WI, US |
| Decision | Substantially Equivalent, Feb 8, 1995 |
| Received | Jan 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950317
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.