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

    HANDTYMP SCREENER MODEL 2000 + 2002 REMOTE TRANS.

    K Number: K890864 · Decision Jun 21, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    69
    Applicant Total
    5
    Review Days
    120

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    Basic Information

    Device Name
    HANDTYMP SCREENER MODEL 2000 + 2002 REMOTE TRANS.
    K Number
    K890864
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.1090
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Applicant
    Rastronics USA, Inc.
    Date Received
    February 21, 1989
    Decision Date
    June 21, 1989
    Product Code
    ETY
    Advisory Committee
    Ear, Nose, Throat
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    ETY Tester, Auditory Impedance

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    Other Clearances by Rastronics USA, Inc.

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