BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇿 New Zealand

    HUMIDIFIER & ACCESSORIES

    K Number: K953949 · Decision Oct 16, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    83
    Registration Numbers
    83
    Same Product Code
    286
    Applicant Total
    17
    Review Days
    55

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    Basic Information

    Device Name
    HUMIDIFIER & ACCESSORIES
    K Number
    K953949
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5440
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Fisher & Paykel Electronics , Ltd.
    Date Received
    August 22, 1995
    Decision Date
    October 16, 1995
    Product Code
    CAW
    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
    CAW Generator, Oxygen, Portable

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