ClearanceBrief
510(k) K963063 ยท LRK Device, Anti-Snoring

SNORE TEC

ApplicantMarketing Technologies, Inc., Bakersfield CA, US
DecisionSubstantially Equivalent, Apr 14, 1997
ReceivedAug 7, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963063

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.