ClearanceBrief
510(k) K130504 ยท LRK Device, Anti-Snoring

ASA ORAL APPLIANCES

ApplicantAmerican Sleep Association, Chesterland OH, US
DecisionSubstantially Equivalent, Oct 18, 2013
ReceivedFeb 27, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130504

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.