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

    PERIPHERAL TRANSLUMINAL ARGIOPLASTY

    K Number: K832279 · Decision Nov 14, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    125

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    Basic Information

    Device Name
    PERIPHERAL TRANSLUMINAL ARGIOPLASTY
    K Number
    K832279
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Sontek Corp.
    Date Received
    July 12, 1983
    Decision Date
    November 14, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Other Clearances by Sontek Corp.

    K Number Device Name
    K831562 SONTEK INFUSION CATHETER
    K810508 SONTEK ANGIOGRAPHIC CATHETER