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

    YOSHIDA RIDO-F, MODEL LM-01

    K Number: K813348 · Decision Jan 7, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    88
    Registration Numbers
    88
    Same Product Code
    88
    Applicant Total
    7
    Review Days
    41

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    Basic Information

    Device Name
    YOSHIDA RIDO-F, MODEL LM-01
    K Number
    K813348
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4200
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Kaycor Intl., Ltd.
    Date Received
    November 27, 1981
    Decision Date
    January 7, 1982
    Product Code
    EKX
    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
    EKX Handpiece, Direct Drive, Ac-Powered

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    Other Clearances by Kaycor Intl., Ltd.

    K Number Device Name
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    K931717 YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY
    K832063 ROBIN CORDLESS HANDPIECE
    K822740 K30000 DENTAL CHAIR
    K811210 YOSHIDA-PANOURA 10
    K811211 YOSHIDA AP 100