BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

    GENERAL (BIOPSY) NEEDLE GUIDE KIT, STERILE

    K Number: K892071 · Decision Aug 8, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    207
    Registration Numbers
    207
    Same Product Code
    360
    Applicant Total
    10
    Review Days
    130

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    Basic Information

    Device Name
    GENERAL (BIOPSY) NEEDLE GUIDE KIT, STERILE
    K Number
    K892071
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1075
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Amedic USA
    Date Received
    March 31, 1989
    Decision Date
    August 8, 1989
    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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