ClearanceBrief
510(k) K962516 ยท LRK Device, Anti-Snoring

TAP ANTI-SNORING DEVICE

ApplicantNellcor Puritan Bennett, Inc., Eden Prairie MN, US
DecisionSubstantially Equivalent, Sep 10, 1996
ReceivedJun 27, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962516

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.