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

    AUDIO 'D' K-AMP HR FULL SHELL AND CANAL HEARING AIDS

    K Number: K962798 · Decision Sep 9, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    101
    Registration Numbers
    101
    Same Product Code
    1366
    Applicant Total
    5
    Review Days
    53

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    Basic Information

    Device Name
    AUDIO 'D' K-AMP HR FULL SHELL AND CANAL HEARING AIDS
    K Number
    K962798
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    874.3300
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Hearing Solutions, Inc.
    Date Received
    July 18, 1996
    Decision Date
    September 9, 1996
    Product Code
    ESD
    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
    ESD Hearing Aid, Air-Conduction, Prescription

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    Other Clearances by Hearing Solutions, Inc.

    K Number Device Name
    K964180 AUDIO 'D' SOUND SELECTOR POWER (SSP)
    K961308 AUDIO 'D' INTIMA CIC
    K960935 AUDIO 'D' 2N SERIES HEARING AIDS(FULL SHELL ITE,HALF SHELL ITE, MINI CANAL, CANAL)
    K944980 SOUND SELECTOR ITE (SSI), BTE (SSB), MINI BTE( SSM)