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

    GAUZE, ABSORBABLE X-RAY DETECT. LAP SPG.

    K Number: K802982 · Decision Dec 19, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    211
    Registration Numbers
    211
    Same Product Code
    110
    Applicant Total
    2
    Review Days
    25

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    Basic Information

    Device Name
    GAUZE, ABSORBABLE X-RAY DETECT. LAP SPG.
    K Number
    K802982
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4450
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Stanford Laboratories
    Date Received
    November 24, 1980
    Decision Date
    December 19, 1980
    Product Code
    GDY
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GDY Gauze/Sponge, Internal, X-Ray Detectable

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