ClearanceBrief
510(k) K140663 ยท LRK Device, Anti-Snoring

THERASNORE

ApplicantDistar, LLC, Albuquerque NM, US
DecisionSubstantially Equivalent, Dec 12, 2014
ReceivedMar 18, 2014
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K140663

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.