BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    DUCPREP BREAST ASPIRATOR, MODEL PMPO2

    K Number: K993342 · Decision Dec 23, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    207
    Registration Numbers
    207
    Same Product Code
    360
    Applicant Total
    2
    Review Days
    79

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    Basic Information

    Device Name
    DUCPREP BREAST ASPIRATOR, MODEL PMPO2
    K Number
    K993342
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1075
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Windy Hill Technology, Inc.
    Date Received
    October 5, 1999
    Decision Date
    December 23, 1999
    Product Code
    KNW
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KNW Instrument, Biopsy

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    Other Clearances by Windy Hill Technology, Inc.

    K Number Device Name
    K983867 FUJI CATHETER, MODEL CTH001