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

    ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV.

    K Number: K893476 · Decision Jun 23, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    136
    Registration Numbers
    136
    Same Product Code
    299
    Applicant Total
    5
    Review Days
    50

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    Basic Information

    Device Name
    ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV.
    K Number
    K893476
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1650
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Andros Analyzers, Inc.
    Date Received
    May 4, 1989
    Decision Date
    June 23, 1989
    Product Code
    JAA
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JAA System, X-Ray, Fluoroscopic, Image-Intensified

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