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

    CORDIPAK ANGIOGRAPHY TRAY

    K Number: K863336 · Decision Sep 12, 1986
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    15

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    Basic Information

    Device Name
    CORDIPAK ANGIOGRAPHY TRAY
    K Number
    K863336
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Angi-Pak Corp.
    Date Received
    August 28, 1986
    Decision Date
    September 12, 1986
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Other Clearances by Angi-Pak Corp.

    K Number Device Name
    K863337 CORDIPAK CARDIAC CATHETERIZATION PACK