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

    COMBINATION 6X-MAGNIFIER AND TWEEZERS

    K Number: K896413 · Decision Feb 1, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    142
    Registration Numbers
    142
    Same Product Code
    14
    Applicant Total
    1
    Review Days
    85

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    Basic Information

    Device Name
    COMBINATION 6X-MAGNIFIER AND TWEEZERS
    K Number
    K896413
    Device Class
    FDA not classified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    James Alexander Corp.
    Date Received
    November 8, 1989
    Decision Date
    February 1, 1990
    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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