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

    CRESCENT TINNITUS RETAINING SOUND GENERATOR

    K Number: K030180 · Decision Sep 17, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    32
    Registration Numbers
    32
    Same Product Code
    76
    Applicant Total
    60
    Review Days
    243

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    Basic Information

    Device Name
    CRESCENT TINNITUS RETAINING SOUND GENERATOR
    K Number
    K030180
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.3400
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Starkey Laboratories, Inc.
    Date Received
    January 17, 2003
    Decision Date
    September 17, 2003
    Product Code
    KLW
    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
    KLW Masker, Tinnitus

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