ClearanceBrief
510(k) K100185 ยท LRK Device, Anti-Snoring

SLEEP APP

ApplicantSleep Medicine Network, Inc., Portland OR, US
DecisionSubstantially Equivalent, Nov 19, 2010
ReceivedJan 22, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100185

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.