ClearanceBrief
510(k) K232804 ยท QME Software For Optical Camera-Based Measurement Of Pulse Rate, Heart Rate, Breathing Rate, And/Or Respiratory Rate

FibriCheck

ApplicantQompium NV, Hasselt, BE
DecisionSubstantially Equivalent, Jun 7, 2024
ReceivedSep 12, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232804

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.