BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

    Anura Mobile Core SDK (M1)

    K Number: K253650 · Decision Jun 11, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    12
    Applicant Total
    1
    Review Days
    203

    Basic Information

    Device Name
    Anura Mobile Core SDK (M1)
    K Number
    K253650
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2785
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Nuralogix Corporation
    Date Received
    November 20, 2025
    Decision Date
    June 11, 2026
    Product Code
    QME
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    QME Software For Optical Camera-Based Measurement Of Pulse Rate, Heart Rate, Breathing Rate, And/Or Respiratory Rate

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