ClearanceBrief
510(k) K970564 ยท IYE Accelerator, Linear, Medical

DYNAMIC WEDGE

ApplicantMitsubishi Electronics America, Inc., Rockville MD, US
DecisionSubstantially Equivalent, May 12, 1997
ReceivedFeb 13, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970564

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.