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

    EAR CURETTE

    K Number: K932609 · Decision Jul 21, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    148
    Registration Numbers
    148
    Same Product Code
    6
    Applicant Total
    2
    Review Days
    54

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    Basic Information

    Device Name
    EAR CURETTE
    K Number
    K932609
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    874.4420
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ear Tech, Inc.
    Date Received
    May 28, 1993
    Decision Date
    July 21, 1993
    Product Code
    JYG
    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
    JYG Curette, Ear

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    Other Clearances by Ear Tech, Inc.

    K Number Device Name
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