ClearanceBrief
510(k) K070327 ยท LRK Device, Anti-Snoring

REMOVABLE ARYLIC HERBST, ALLESEE SNORE APPLIANCE (ASA), AND ENOCH SNORINATOR

ApplicantSybron Dental Specialties, Inc., Orange CA, US
DecisionSubstantially Equivalent, May 25, 2007
ReceivedFeb 5, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070327

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.