ClearanceBrief
510(k) K802941 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic

CINESCOPE III RADIOGRAPHIC GENERATOR

ApplicantControtec, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 9, 1981
ReceivedNov 19, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802941

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.