BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    Hypertension Notification Feature (HTNF)

    K Number: K250507 · Decision Sep 11, 2025
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1
    Same Product Code
    0
    Applicant Total
    12
    Review Days
    202

    Basic Information

    Device Name
    Hypertension Notification Feature (HTNF)
    K Number
    K250507
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2380
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Apple, Inc.
    Date Received
    February 21, 2025
    Decision Date
    September 11, 2025
    Product Code
    SFR
    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
    SFR Hypertension Machine Learning-Based Notification Software

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