ClearanceBrief
510(k) K160531 ยท LRK Device, Anti-Snoring

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ApplicantFirma Ingemarsson, Charlottenlund, DK
DecisionSubstantially Equivalent, Sep 1, 2016
ReceivedFeb 25, 2016
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K160531

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.