ClearanceBrief
510(k) K162748 ยท LXJ Interactive Rehabilitation Exercise Devices

MindMotionPRO

ApplicantMindmaze SA, Lausanne, CH
DecisionSubstantially Equivalent, Apr 24, 2017
ReceivedSep 30, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K162748

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.