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

    ERYTHROCATH UMBILICAL CATHETER

    K Number: K841880 · Decision Jan 14, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    212
    Registration Numbers
    213
    Same Product Code
    496
    Applicant Total
    2
    Review Days
    252

    Basic Information

    Device Name
    ERYTHROCATH UMBILICAL CATHETER
    K Number
    K841880
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    CARDIOSEARCH, INC.
    Date Received
    May 7, 1984
    Decision Date
    January 14, 1985
    Product Code
    FOZ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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    Other Clearances by CARDIOSEARCH, INC.

    K Number Device Name
    K842133 EYRTHROCATH DOUBLE-LUMEN CENTRAL VENOUS