ClearanceBrief
510(k) K171547 ยท LXJ Interactive Rehabilitation Exercise Devices

Qualisys Clinical System

ApplicantQualisys AB, Goteborg, SE
DecisionSubstantially Equivalent, Aug 2, 2018
ReceivedMay 26, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171547

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.