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

    SKILCRAFT

    K Number: K880785 · Decision Mar 11, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    329
    Registration Numbers
    330
    Same Product Code
    61
    Applicant Total
    2
    Review Days
    14

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    Basic Information

    Device Name
    SKILCRAFT
    K Number
    K880785
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Pennsylvania Association For the Blind
    Date Received
    February 26, 1988
    Decision Date
    March 11, 1988
    Product Code
    KDD
    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
    KDD Kit, Surgical Instrument, Disposable

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    Other Clearances by Pennsylvania Association For the Blind

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    K903486 MASK, SURGICAL-DISPOSABLE NSN 6510-00-982-7493