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

    EPIDURAL BLOCK PROCEDURE PACK

    K Number: K770096 · Decision Feb 25, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    81
    Registration Numbers
    81
    Same Product Code
    154
    Applicant Total
    10
    Review Days
    39

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    Basic Information

    Device Name
    EPIDURAL BLOCK PROCEDURE PACK
    K Number
    K770096
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5140
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    American Viggo
    Date Received
    January 17, 1977
    Decision Date
    February 25, 1977
    Product Code
    CAZ
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CAZ Anesthesia Conduction Kit

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