ClearanceBrief
510(k) K122475 ยท LRK Device, Anti-Snoring

ZQUIET PRO-PLUS

ApplicantSleeping Well, LLC, Shelburne VT, US
DecisionSubstantially Equivalent, Dec 7, 2012
ReceivedAug 14, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122475

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.