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

    ANGIOSCANE SPECTRUM ANALYZER

    K Number: K834501 · Decision May 23, 1984
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    154

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    Basic Information

    Device Name
    ANGIOSCANE SPECTRUM ANALYZER
    K Number
    K834501
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Unigon Industries, Inc.
    Date Received
    December 21, 1983
    Decision Date
    May 23, 1984
    Advisory Committee
    Unknown
    Review Advisory Committee
    NE
    Third Party
    N

    Other Clearances by Unigon Industries, Inc.

    K Number Device Name
    K834525 ANGIOSCAN FLO MAD SPECTRUM ANALYZER
    K812184 ANGIOSCAN SPECTRUM ANALYZER