510(k) K933650 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic
PHILIPS XRG 90 X-RAY GENERATOR SYSTEM
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Oct 7, 1993 |
| Received | Jul 27, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933650
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.