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

    PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV

    K Number: K890182 · Decision Feb 28, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    26
    Registration Numbers
    26
    Same Product Code
    187
    Applicant Total
    13
    Review Days
    406

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    Basic Information

    Device Name
    PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV
    K Number
    K890182
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.3450
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Aesculap Instruments Corp.
    Date Received
    January 18, 1989
    Decision Date
    February 28, 1990
    Product Code
    DSY
    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
    DSY Prosthesis, Vascular Graft, Of 6mm And Greater Diameter

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