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

    Air Compression Therapy System

    K Number: K192466 · Decision Jun 22, 2020
    View on FDA
    Classifications
    1
    FEI Numbers
    95
    Registration Numbers
    95
    Same Product Code
    152
    Applicant Total
    2
    Review Days
    287

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    Basic Information

    Device Name
    Air Compression Therapy System
    K Number
    K192466
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5650
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Shenzhen Lifotronic Technology Co., Ltd.
    Date Received
    September 9, 2019
    Decision Date
    June 22, 2020
    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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    Other Clearances by Shenzhen Lifotronic Technology Co., Ltd.

    K Number Device Name
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