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

    AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT

    K Number: K883522 · Decision Sep 30, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    6
    Applicant Total
    5
    Review Days
    44

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    Basic Information

    Device Name
    AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT
    K Number
    K883522
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Amerimed US Corp.
    Date Received
    August 17, 1988
    Decision Date
    September 30, 1988
    Product Code
    LBK
    Advisory Committee
    Unknown
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LBK Neurosurgical Ultrasonic Instruments

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