ClearanceBrief
510(k) K113126 ยท LRK Device, Anti-Snoring

ACRYLIC HERBST APPLIANCE

ApplicantGergens Orthodontic Lab, Dunlap IL, US
DecisionSubstantially Equivalent, Jul 17, 2013
ReceivedOct 24, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113126

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.