ClearanceBrief
510(k) K210910 ยท LRK Device, Anti-Snoring

Snore Bandit

ApplicantSnorebandit, LLC, Las Vegas NV, US
DecisionSubstantially Equivalent, Jul 1, 2021
ReceivedMar 29, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210910

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.