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

    PFM PROFESSIONAL 7000 SPIROMETER

    K Number: K932278 · Decision Dec 17, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    62
    Applicant Total
    10
    Review Days
    219

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    Basic Information

    Device Name
    PFM PROFESSIONAL 7000 SPIROMETER
    K Number
    K932278
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.1890
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Advanced Medical Systems, Inc.
    Date Received
    May 12, 1993
    Decision Date
    December 17, 1993
    Product Code
    BTY
    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
    BTY Calculator, Predicted Values, Pulmonary Function

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