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

    RITTER MODEL J DENTAL CHAIR

    K Number: K800084 · Decision Jan 29, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    14
    Registration Numbers
    14
    Same Product Code
    62
    Applicant Total
    10
    Review Days
    15

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    Basic Information

    Device Name
    RITTER MODEL J DENTAL CHAIR
    K Number
    K800084
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6250
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Ritter Co.
    Date Received
    January 14, 1980
    Decision Date
    January 29, 1980
    Product Code
    KLC
    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
    KLC Chair, Dental, With Operative Unit

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