ClearanceBrief
510(k) K090436 ยท LRK Device, Anti-Snoring

AIRWAYEASE MAS

ApplicantOrthoplant Dental Lab, Bella Vista, New South Wales, AU
DecisionSubstantially Equivalent, Apr 16, 2010
ReceivedFeb 19, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090436

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.