ClearanceBrief
510(k) K950763 ยท LRK Device, Anti-Snoring

LOWE KLEARWAY

ApplicantDr. Alan A. Lowe, Inc., Vancouver, B.C. V6k 4m1, CA
DecisionSubstantially Equivalent, May 25, 1995
ReceivedFeb 17, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950763

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.