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

    OPTICHAMBER DIAMOND VALVED HOLDING CHAMBER

    K Number: K110293 · Decision Aug 9, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    26
    Registration Numbers
    26
    Same Product Code
    15
    Applicant Total
    5
    Review Days
    189

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    Basic Information

    Device Name
    OPTICHAMBER DIAMOND VALVED HOLDING CHAMBER
    K Number
    K110293
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5630
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Respironics New Jersey, Inc.
    Date Received
    February 1, 2011
    Decision Date
    August 9, 2011
    Product Code
    NVP
    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
    NVP Holding Chambers, Direct Patient Interface

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