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

    AIRSTRIP RPM FOR LIFENET CONSULT

    K Number: K121712 · Decision Nov 20, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    72
    Registration Numbers
    72
    Same Product Code
    116
    Applicant Total
    5
    Review Days
    162

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    Basic Information

    Device Name
    AIRSTRIP RPM FOR LIFENET CONSULT
    K Number
    K121712
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2300
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Airstrip Technologies, Inc.
    Date Received
    June 11, 2012
    Decision Date
    November 20, 2012
    Product Code
    MSX
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MSX System, Network And Communication, Physiological Monitors

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