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

    DERMAL GLOVES

    K Number: K932953 · Decision Jun 24, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    877
    Registration Numbers
    878
    Same Product Code
    55
    Applicant Total
    1
    Review Days
    372

    Basic Information

    Device Name
    DERMAL GLOVES
    K Number
    K932953
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4040
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    GEORGE GLOVE COMPANY, INC.
    Date Received
    June 17, 1993
    Decision Date
    June 24, 1994
    Product Code
    LYU
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LYU Accessory, Surgical Apparel

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