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

    KAVO QUATTROCARE

    K Number: K012308 · Decision Jun 26, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    89
    Registration Numbers
    89
    Same Product Code
    260
    Applicant Total
    20
    Review Days
    338

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    Basic Information

    Device Name
    KAVO QUATTROCARE
    K Number
    K012308
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4200
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Kavo America
    Date Received
    July 23, 2001
    Decision Date
    June 26, 2002
    Product Code
    EFB
    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
    EFB Handpiece, Air-Powered, Dental

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    Other Clearances by Kavo America

    K Number Device Name
    K073074 KEY LASER III 1243 US WITH DETECT
    K072262 GENTLERAY 980 DIODE LASER SYSTEM
    K063624 KAVO EVEREST C-TEMP
    K051909 DIAGNODENT
    K030146 KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+
    K050019 IN EXAM INTRAORAL DENTAL X-RAY SYSTEM
    K032081 KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60
    K031868 PROPHYPEARLS
    K030607 KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND COLORINGS/STAINING/SHADES
    K024214 KAVO EVEREST TITANBLANK
    Search all 20 clearances from Kavo America →