BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    Vivatmo pro

    K Number: K233775 · Decision Feb 22, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    14
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    Vivatmo pro
    K Number
    K233775
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3080
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Bosch Healthcare Solutions GmbH
    Date Received
    November 24, 2023
    Decision Date
    February 22, 2024
    Product Code
    MXA
    Advisory Committee
    Clinical Toxicology
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MXA System, Test, Breath Nitric Oxide

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    Other Clearances by Bosch Healthcare Solutions GmbH

    K Number Device Name
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