BEUDAMED
    FDA 510(k) FDA not classified Unknown 🇺🇸 United States

    AUTO FIRST-AID KIT FOR AMERICA

    K Number: K903393 · Decision Jan 31, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    142
    Registration Numbers
    142
    Same Product Code
    14
    Applicant Total
    1
    Review Days
    188

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    Basic Information

    Device Name
    AUTO FIRST-AID KIT FOR AMERICA
    K Number
    K903393
    Device Class
    FDA not classified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Unknown
    Applicant
    Hisler-Radke, Inc.
    Date Received
    July 27, 1990
    Decision Date
    January 31, 1991
    Product Code
    LRR
    Advisory Committee
    Unknown
    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
    LRR First Aid Kit With Drug

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