510(k) K880352 ยท KPR System, X-Ray, Stationary
MTX GENERATOR
| Applicant | Philips Medical Systems (Cleveland), Inc., Highland Heights OH, US |
| Decision | Substantially Equivalent, Jul 14, 1988 |
| Received | Jan 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880352
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.