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

    CHIN UP

    K Number: K943837 · Decision Oct 14, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    279
    Registration Numbers
    280
    Same Product Code
    7
    Applicant Total
    1
    Review Days
    70

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    Basic Information

    Device Name
    CHIN UP
    K Number
    K943837
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.6820
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Edward Carden
    Date Received
    August 5, 1994
    Decision Date
    October 14, 1994
    Product Code
    CCX
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CCX Support, Patient Position

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