ClearanceBrief
510(k) K173931 ยท LXJ Interactive Rehabilitation Exercise Devices

MindMotion(TM) GO

ApplicantMindmaze SA, Lausanne, CH
DecisionSubstantially Equivalent, May 17, 2018
ReceivedDec 26, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173931

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.