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

    SONTEK ANGIOGRAPHIC CATHETER

    K Number: K810508 · Decision Apr 17, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    210
    Registration Numbers
    211
    Same Product Code
    499
    Applicant Total
    3
    Review Days
    52

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    Basic Information

    Device Name
    SONTEK ANGIOGRAPHIC CATHETER
    K Number
    K810508
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1200
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Sontek Corp.
    Date Received
    February 24, 1981
    Decision Date
    April 17, 1981
    Product Code
    DQO
    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
    DQO Catheter, Intravascular, Diagnostic

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    Other Clearances by Sontek Corp.

    K Number Device Name
    K832279 PERIPHERAL TRANSLUMINAL ARGIOPLASTY
    K831562 SONTEK INFUSION CATHETER