ClearanceBrief
510(k) K112205 ยท LRK Device, Anti-Snoring

SNORERX 9.0

ApplicantConsumer Health Products, Inc., Aliso Viejo CA, US
DecisionSubstantially Equivalent, Nov 16, 2011
ReceivedAug 1, 2011
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K112205

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.