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

    DISPOS. MONITORING SYS/LI ET AL

    K Number: K820201 · Decision Feb 12, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    87
    Registration Numbers
    87
    Same Product Code
    147
    Applicant Total
    5
    Review Days
    17

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    Basic Information

    Device Name
    DISPOS. MONITORING SYS/LI ET AL
    K Number
    K820201
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2850
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Linton Biomed Corp.
    Date Received
    January 26, 1982
    Decision Date
    February 12, 1982
    Product Code
    DRS
    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
    DRS Transducer, Blood-Pressure, Extravascular

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