ClearanceBrief
510(k) K252942 ยท LRK Device, Anti-Snoring

ShaeferH

ApplicantShaeferh, LLC, Boston MA, US
DecisionSubstantially Equivalent, Apr 10, 2026
ReceivedSep 15, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K252942

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.