BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇷 Greece

    LANGGASSE 90

    K Number: K932470 · Decision Aug 25, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    21
    Registration Numbers
    21
    Same Product Code
    31
    Applicant Total
    1
    Review Days
    97

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    Basic Information

    Device Name
    LANGGASSE 90
    K Number
    K932470
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    874.5300
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Happersberger Otopront GmbH
    Date Received
    May 20, 1993
    Decision Date
    August 25, 1993
    Product Code
    ETF
    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
    ETF Unit, Examining/Treatment, Ent

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