BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

    IN SITU EAR GAIN AUDIO TEST STAT TYPE 2118/WH 1823

    K Number: K862086 · Decision Jul 16, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    15
    Registration Numbers
    15
    Same Product Code
    45
    Applicant Total
    1
    Review Days
    44

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    Basic Information

    Device Name
    IN SITU EAR GAIN AUDIO TEST STAT TYPE 2118/WH 1823
    K Number
    K862086
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.3310
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Applicant
    A/S Bruel & Kjaer
    Date Received
    June 2, 1986
    Decision Date
    July 16, 1986
    Product Code
    ETW
    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
    ETW Calibrator, Hearing Aid / Earphone And Analysis Systems

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