BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Air Compression Therapy Device (K1002/K1006/K1007/K1008/K1061)

    K Number: K251623 · Decision Sep 17, 2025
    View on FDA
    Classifications
    1
    FEI Numbers
    95
    Registration Numbers
    95
    Same Product Code
    152
    Applicant Total
    3
    Review Days
    112

    Basic Information

    Device Name
    Air Compression Therapy Device (K1002/K1006/K1007/K1008/K1061)
    K Number
    K251623
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5650
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Shenzhen Yicai Health Technology Co., Ltd.
    Date Received
    May 28, 2025
    Decision Date
    September 17, 2025
    Product Code
    IRP
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IRP Massager, Powered Inflatable Tube

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