BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    PRESSURE MONITOR, MODEL 212

    K Number: K790302 · Decision Mar 21, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    46
    Registration Numbers
    46
    Same Product Code
    11
    Applicant Total
    1
    Review Days
    36

    Basic Information

    Device Name
    PRESSURE MONITOR, MODEL 212
    K Number
    K790302
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    888.1250
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Applicant
    Zatek
    Date Received
    February 13, 1979
    Decision Date
    March 21, 1979
    Product Code
    HRW
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HRW Dynamometer, Nonpowered

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