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

    TRANSENDOSCOPIC INJECTION CATHETER TEI

    K Number: K821336 · Decision May 21, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    38
    Registration Numbers
    38
    Same Product Code
    63
    Applicant Total
    1
    Review Days
    16

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    Basic Information

    Device Name
    TRANSENDOSCOPIC INJECTION CATHETER TEI
    K Number
    K821336
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5130
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Sounson Research Co., Inc.
    Date Received
    May 5, 1982
    Decision Date
    May 21, 1982
    Product Code
    KNY
    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
    KNY Accessories, Catheter, G-U

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