BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    NON INVASIVE VASCULAR PROGRAM

    K Number: K932852 · Decision Feb 4, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    0
    Applicant Total
    19
    Review Days
    239

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    Basic Information

    Device Name
    NON INVASIVE VASCULAR PROGRAM
    K Number
    K932852
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1815
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    D. E. Hokanson, Inc.
    Date Received
    June 10, 1993
    Decision Date
    February 4, 1994
    Product Code
    JOB
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JOB Hexane Extraction, Fluorescence, Vitamin E

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