ClearanceBrief
510(k) K961214 ยท IYE Accelerator, Linear, Medical

MULTI LEAF COLLIMATOR

ApplicantMitsubishi Intl. Corp., Conshohocken PA, US
DecisionSubstantially Equivalent, Aug 6, 1996
ReceivedMar 28, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961214

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.