BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Disposable Biopsy Valve

    K Number: K173758 · Decision May 14, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    98
    Registration Numbers
    98
    Same Product Code
    92
    Applicant Total
    13
    Review Days
    154

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    Basic Information

    Device Name
    Disposable Biopsy Valve
    K Number
    K173758
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Zhejiang Chuangxiang Medical Technology Co., Ltd.
    Date Received
    December 11, 2017
    Decision Date
    May 14, 2018
    Product Code
    OCX
    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
    OCX Endoscopic Irrigation/Suction System

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    Other Clearances by Zhejiang Chuangxiang Medical Technology Co., Ltd.

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    K220063 Single Use Cytology Brush
    K212669 Single Use Hemoclip
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    K212668 Sclerotherapy Needle
    K191900 Single Use Grasping Forceps
    K192258 Disposable Valve Sets
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