ClearanceBrief
510(k) K240929 ยท QZW Over-The-Counter Device To Assess Risk Of Sleep Apnea

Sleep Apnea Notification Feature (SANF)

ApplicantApple, Inc., Cupertino CA, US
DecisionSubstantially Equivalent, Sep 13, 2024
ReceivedApr 4, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240929

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.