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    FDA 510(k) FDA class 1 Substantially Equivalent 🇹🇼 Taiwan

    KARMA MANUAL WHEELCHAIR, MODELS S-ERGO 305 AND S-ERGO 105

    K Number: K062309 · Decision Oct 10, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    129
    Registration Numbers
    129
    Same Product Code
    458
    Applicant Total
    5
    Review Days
    63

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    Basic Information

    Device Name
    KARMA MANUAL WHEELCHAIR, MODELS S-ERGO 305 AND S-ERGO 105
    K Number
    K062309
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3850
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Karma Medical Products Co., Ltd.
    Date Received
    August 8, 2006
    Decision Date
    October 10, 2006
    Product Code
    IOR
    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
    IOR Wheelchair, Mechanical

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