ClearanceBrief
510(k) K170825 ยท LRK Device, Anti-Snoring

SnoreRx

ApplicantApnea Sciences Corporation, Aliso Viejo CA, US
DecisionSubstantially Equivalent, Aug 18, 2017
ReceivedMar 20, 2017
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K170825

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.