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

    ORIGINAL TICK KIT/1ST AID KIT

    K Number: K895767 · Decision Dec 22, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    142
    Registration Numbers
    142
    Same Product Code
    14
    Applicant Total
    1
    Review Days
    86

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    Basic Information

    Device Name
    ORIGINAL TICK KIT/1ST AID KIT
    K Number
    K895767
    Device Class
    FDA not classified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Unknown
    Applicant
    Tick Kit, Inc.
    Date Received
    September 27, 1989
    Decision Date
    December 22, 1989
    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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