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

    MAGELLAN VENTILATOR

    K Number: K002951 · Decision Dec 8, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    4
    Review Days
    78

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    Basic Information

    Device Name
    MAGELLAN VENTILATOR
    K Number
    K002951
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5895
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Oceanic Medical Products, Inc.
    Date Received
    September 21, 2000
    Decision Date
    December 8, 2000
    Product Code
    CBK
    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
    CBK Ventilator, Continuous, Facility Use

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    Other Clearances by Oceanic Medical Products, Inc.

    K Number Device Name
    K072420 MAGELLAN-2200, MODEL-3 ANESTHESIA MACHINE
    K060193 MAGELLAN-2200 MODEL -2 ANESTHESIA MACHINE, MODEL 2
    K010613 MAGELLAN-2200, MODEL 1