ClearanceBrief
510(k) K970303 ยท IXI Block, Beam-Shaping, Radiation Therapy

SATURNE MULTILEAF COLLIMATOR

ApplicantGeneral Electric Co., Milwaukee WI, US
DecisionSubstantially Equivalent, Apr 25, 1997
ReceivedJan 27, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970303

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.