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

    DEROYAL INDUSTRIES, INC. DEFOGGER

    K Number: K982465 · Decision Aug 11, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    64
    Registration Numbers
    64
    Same Product Code
    26
    Applicant Total
    91
    Review Days
    27

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    Basic Information

    Device Name
    DEROYAL INDUSTRIES, INC. DEFOGGER
    K Number
    K982465
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Deroyal Industries, Inc.
    Date Received
    July 15, 1998
    Decision Date
    August 11, 1998
    Product Code
    OCT
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OCT Anti Fog Solution And Accessories, Endoscopy

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