510(k) K800554 ยท IXL Device, Spot-Film
MULTI-FORMAT SFD MODEL 1720
| Applicant | Philips Medical Systems (Cleveland), Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 10, 1980 |
| Received | Mar 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800554
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.