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

    VASCULAR BIOPSY FORCEPS

    K Number: K910840 · Decision Jul 15, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    25
    Registration Numbers
    25
    Same Product Code
    22
    Applicant Total
    3
    Review Days
    138

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    Basic Information

    Device Name
    VASCULAR BIOPSY FORCEPS
    K Number
    K910840
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4075
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Vascular Products, Inc.
    Date Received
    February 27, 1991
    Decision Date
    July 15, 1991
    Product Code
    DWZ
    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
    DWZ Device, Biopsy, Endomyocardial

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    Other Clearances by Vascular Products, Inc.

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