BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

    GONIOMETER AND BIOMEDICAL RECORDER SYSTEM

    K Number: K884003 · Decision Dec 19, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    45
    Registration Numbers
    45
    Same Product Code
    32
    Applicant Total
    1
    Review Days
    89

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    Basic Information

    Device Name
    GONIOMETER AND BIOMEDICAL RECORDER SYSTEM
    K Number
    K884003
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    888.1500
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Applicant
    Penny & Giles Blackwood , Ltd.
    Date Received
    September 21, 1988
    Decision Date
    December 19, 1988
    Product Code
    KQX
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KQX Goniometer, Ac-Powered

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