BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    ULTRAGARD IMPERVIOUS REINFORCED GOWN

    K Number: K013846 · Decision May 22, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    222
    Registration Numbers
    222
    Same Product Code
    294
    Applicant Total
    1
    Review Days
    183

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    Basic Information

    Device Name
    ULTRAGARD IMPERVIOUS REINFORCED GOWN
    K Number
    K013846
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4040
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Precept Medical Products, Inc.
    Date Received
    November 20, 2001
    Decision Date
    May 22, 2002
    Product Code
    FYA
    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
    FYA Gown, Surgical

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