BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    ZEFON ADULT ANESTHESIA BREATHING CIRCUIT

    K Number: K911880 · Decision Dec 20, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    199
    Registration Numbers
    199
    Same Product Code
    183
    Applicant Total
    4
    Review Days
    235

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    Basic Information

    Device Name
    ZEFON ADULT ANESTHESIA BREATHING CIRCUIT
    K Number
    K911880
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.5240
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Bill Olson Corp.
    Date Received
    April 29, 1991
    Decision Date
    December 20, 1991
    Product Code
    CAI
    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
    CAI Circuit, Breathing (W Connector, Adaptor, Y Piece)

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    Other Clearances by Bill Olson Corp.

    K Number Device Name
    K973238 ZEFON ADULT ANESTHESIA BREATHING CIRCUIT WITH FILTER, ZEFON PEDIATRIC ANESTHESIA BREATHING CIRCUIT WITH FILTER
    K935168 ZEFON PEDIATRIC ANESTHESIA BREATHING CIRCUIT KITS
    K911651 ZEFON BATERIAL/VIRAL FILTER