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

    ADT DISPOSABLE THIN NEEDLE(SKINNY CHIBA)

    K Number: K800416 · Decision Mar 25, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    128
    Registration Numbers
    128
    Same Product Code
    132
    Applicant Total
    21
    Review Days
    28

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    Basic Information

    Device Name
    ADT DISPOSABLE THIN NEEDLE(SKINNY CHIBA)
    K Number
    K800416
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1075
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    A.D.T. Lab Industries
    Date Received
    February 26, 1980
    Decision Date
    March 25, 1980
    Product Code
    FCG
    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
    FCG Biopsy Needle

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    Other Clearances by A.D.T. Lab Industries

    K Number Device Name
    K812297 A.D.T. PROCEDURES TRAY
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    K801753 ADT BONE MARROW BIOPSY-ASPIR. NEELDE
    K800410 ADT BONE MARROW BIOPSY-ASPIRATION TRAY
    K800417 ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL
    K800411 ASPIRATION TRAY W/FERRIS DISP. ILLINOIS
    K800418 ADT DISPOSABLE THIN NEEDLE ASPIRATION
    K800414 ADT SOFT TISSUE BIOPSY TRAY
    K800408 ADT BONE MAR. BIO/ASP. TRAY W/NEEDLE
    K800409 ADT BONE MARROW BIOPSY ASPIRATION TRAY
    Search all 21 clearances from A.D.T. Lab Industries →