ClearanceBrief
510(k) K950037 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic

N 800 HF

ApplicantOldelft Corp. of America, Fairfax VA, US
DecisionSubstantially Equivalent, Feb 15, 1995
ReceivedJan 4, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950037

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.