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

    GROUP AUDITORY TRAINING SYSTEM

    K Number: K922720 · Decision Aug 24, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    31
    Applicant Total
    31
    Review Days
    80

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    Basic Information

    Device Name
    GROUP AUDITORY TRAINING SYSTEM
    K Number
    K922720
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.3320
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Phonic Ear, Inc.
    Date Received
    June 5, 1992
    Decision Date
    August 24, 1992
    Product Code
    EPF
    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
    EPF Hearing Aid, Group And Auditory Trainer

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    Other Clearances by Phonic Ear, Inc.

    K Number Device Name
    K043090 EASYLISTENER 2 FM, RADIUM FM AND VOCALIGHT INFRARED SOUND FIELD SYSTEMS
    K974658 INFRARED GROUP AMPLIFICATION SYSTEM, INFRARED EMITTER, INFRARED BODY WORN RECEIVER, INFRARED HEADSET RECEIVER-STEREO, IT
    K974287 FM RECEIVER - AUDITORY TRAINER
    K950730 GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM)
    K940313 PHONIC EAR
    K923234 PE 400IR, PE 400T, PE 400E
    K912356 GROUP AUDITORY TRAINER,FM RECEIVER
    K893431 AUDITORY TRAINER PE150R FM RECEIVER
    K882409 PE100R FM RECEIVER USED W/PE100T FM TRANSMITTER
    K881099 PE485R FM RECEIVER USED W/PE481FST FM TRANSMITTER
    Search all 31 clearances from Phonic Ear, Inc. →