BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    KENDRICK EXTRICATION DEVICE

    K Number: K781761 · Decision Oct 27, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    78
    Registration Numbers
    78
    Same Product Code
    6
    Applicant Total
    1
    Review Days
    11

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    Basic Information

    Device Name
    KENDRICK EXTRICATION DEVICE
    K Number
    K781761
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3490
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Medi-Ked, Inc.
    Date Received
    October 16, 1978
    Decision Date
    October 27, 1978
    Product Code
    IQF
    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
    IQF Orthosis, Cervical-Thoracic, Rigid

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