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

    TRAVENOL MULTIDAY INFUSOR 2C1080

    K Number: K842905 · Decision Nov 1, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    149
    Registration Numbers
    149
    Same Product Code
    847
    Applicant Total
    206
    Review Days
    465

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    Basic Information

    Device Name
    TRAVENOL MULTIDAY INFUSOR 2C1080
    K Number
    K842905
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Travenol Laboratories, S.A.
    Date Received
    July 24, 1984
    Decision Date
    November 1, 1985
    Product Code
    FRN
    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
    FRN Pump, Infusion

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    Other Clearances by Travenol Laboratories, S.A.

    K Number Device Name
    K874181 BAXTER BEDSIDE SYSTEM
    K873894 CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITE
    K873873 RESUBMITTED MICRON TRANSFUSION FILTER
    K873984 AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)
    K872364 HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309
    K872652 UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM
    K870801 FLO-GARD 6200 VOLUMETRIC INFUSION/PUMPING BLOOD
    K871908 IV ADMINISTRATION SET
    K871471 CAPILLARY FLOW DIALYZERS MODELS ST-12 & ST-15
    K865029 CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER
    Search all 206 clearances from Travenol Laboratories, S.A. →