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

    FIBER OPTIC HOSE

    K Number: K801592 · Decision Jul 21, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    24
    Registration Numbers
    24
    Same Product Code
    17
    Applicant Total
    6
    Review Days
    10

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    Basic Information

    Device Name
    FIBER OPTIC HOSE
    K Number
    K801592
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4620
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Lares Manufacturing Co., Inc.
    Date Received
    July 11, 1980
    Decision Date
    July 21, 1980
    Product Code
    EAY
    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
    EAY Light, Fiber Optic, Dental

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    Other Clearances by Lares Manufacturing Co., Inc.

    K Number Device Name
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    K801535 LARES HANDPIECE OIL
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