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

    VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM

    K Number: K935778 · Decision Dec 5, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    22
    Applicant Total
    4
    Review Days
    1098

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    Basic Information

    Device Name
    VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM
    K Number
    K935778
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.1200
    Medical Specialty
    Anesthesiology
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Via Medical Corp.
    Date Received
    December 3, 1993
    Decision Date
    December 5, 1996
    Product Code
    CCE
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CCE Analyzer, Gas, Oxygen, Partial Pressure, Blood-Phase, Indwelling

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    Other Clearances by Via Medical Corp.

    K Number Device Name
    K951739 PUMP/BLOOD CHEMISTRY MONITOR
    K922997 VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.
    K920438 VIA 1-01 INFUSION PUMP BLOOD CHEMISTRY SYSTEM