BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇭🇰 Hong Kong

    PanopticAI Vital Signs (1.6.1-22)

    K Number: K260066 · Decision May 21, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    12
    Applicant Total
    1
    Review Days
    132

    Basic Information

    Device Name
    PanopticAI Vital Signs (1.6.1-22)
    K Number
    K260066
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2785
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    PanopticAI Technologies Limited
    Date Received
    January 9, 2026
    Decision Date
    May 21, 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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