ClearanceBrief
510(k) K890083 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic

GX-2000 STATIONARY X-RAY GENERATOR

ApplicantGendex Corp., Franklin Park IL, US
DecisionSubstantially Equivalent, Mar 31, 1989
ReceivedJan 10, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890083

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.