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

    MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY

    K Number: K072061 · Decision Apr 22, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    10
    Applicant Total
    14
    Review Days
    270

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    Basic Information

    Device Name
    MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY
    K Number
    K072061
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.1760
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Viasys Healthcare GmbH
    Date Received
    July 27, 2007
    Decision Date
    April 22, 2008
    Product Code
    JEH
    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
    JEH Plethysmograph, Volume

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    Other Clearances by Viasys Healthcare GmbH

    K Number Device Name
    K092324 SPIROPRO
    K091412 CLEAN PEAK FLOW METER
    K091505 COR12+
    K081823 MASTERSCREEN PAED - BABY BODY
    K080510 VIP PULMONARY FUNCTION SYSTEM
    K080734 FLOWSCREEN, FLOWSCREEN/CORSCREEN, FLOWSCREEN CT
    K072323 MASTERSCREEN & OXYCON CPX
    K071753 MASTERSCREEN PNEUMO & MASTERSCOPE
    K062011 MODIFICATION TO FLOWSCREEN
    K070614 CORSCREEN
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