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

    NEICH NM ADVANCE CATHETER SHEATH INTRODUCER

    K Number: K020964 · Decision Oct 11, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    273
    Registration Numbers
    273
    Same Product Code
    701
    Applicant Total
    1
    Review Days
    200

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    Basic Information

    Device Name
    NEICH NM ADVANCE CATHETER SHEATH INTRODUCER
    K Number
    K020964
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1340
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Neich Medical(Shenzhen)Company, Ltd.
    Date Received
    March 25, 2002
    Decision Date
    October 11, 2002
    Product Code
    DYB
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DYB Introducer, Catheter

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