510(k) K925105 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
PHILIPS MEDIO CP FAMILY
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Dec 28, 1992 |
| Received | Oct 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925105
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.