ClearanceBrief
510(k) K090503 ยท LRK Device, Anti-Snoring

ZQUIET MOUTHPIECE

ApplicantSleeping Well, LLC, Crofton MD, US
DecisionSubstantially Equivalent, Mar 10, 2009
ReceivedFeb 25, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090503

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.