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

    ACCESSORY TO EYEDROP GUIDE

    K Number: K884974 · Decision Mar 24, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    67
    Registration Numbers
    67
    Same Product Code
    4
    Applicant Total
    2
    Review Days
    114

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    Basic Information

    Device Name
    ACCESSORY TO EYEDROP GUIDE
    K Number
    K884974
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    874.4420
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Applicant
    Suredrop, Inc.
    Date Received
    November 30, 1988
    Decision Date
    March 24, 1989
    Product Code
    JYJ
    Advisory Committee
    Ear, Nose, Throat
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JYJ Gauge, Measuring

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    Other Clearances by Suredrop, Inc.

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