ClearanceBrief
510(k) K253650 ยท QME Software For Optical Camera-Based Measurement Of Pulse Rate, Heart Rate, Breathing Rate, And/Or Respiratory Rate

Anura Mobile Core SDK (M1)

ApplicantNuralogix Corporation, Toronto, CA
DecisionSubstantially Equivalent, Jun 11, 2026
ReceivedNov 20, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253650

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.