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

    COGAN CORP KITS OF DENTAL HAND INSTRUMENTS

    K Number: K915299 · Decision Jan 31, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    56
    Registration Numbers
    56
    Same Product Code
    23
    Applicant Total
    1
    Review Days
    73

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    Basic Information

    Device Name
    COGAN CORP KITS OF DENTAL HAND INSTRUMENTS
    K Number
    K915299
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.3165
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Cogan Corp.
    Date Received
    November 19, 1991
    Decision Date
    January 31, 1992
    Product Code
    EGG
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    EGG Attachment, Precision, All

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