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

    VENDYS MODEL 5000 B/BC

    K Number: K060980 · Decision Aug 16, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    178
    Registration Numbers
    178
    Same Product Code
    429
    Applicant Total
    2
    Review Days
    493

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    Basic Information

    Device Name
    VENDYS MODEL 5000 B/BC
    K Number
    K060980
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1425
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Endothelix, Inc.
    Date Received
    April 10, 2006
    Decision Date
    August 16, 2007
    Product Code
    DQK
    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
    DQK Computer, Diagnostic, Programmable

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    Other Clearances by Endothelix, Inc.

    K Number Device Name
    K072919 VENDYS, MODEL 6000 B B/C