ClearanceBrief
510(k) K914302 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic

GEN-X 800/650

ApplicantSwissray Finatech, Inc., Mobile AL, US
DecisionSubstantially Equivalent, Oct 30, 1991
ReceivedSep 25, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914302

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.