BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    SUNSOR ULTRAVIOLET METER

    K Number: K934728 · Decision Jul 28, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    1
    Applicant Total
    1
    Review Days
    302

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    Basic Information

    Device Name
    SUNSOR ULTRAVIOLET METER
    K Number
    K934728
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.6350
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sunsor, Inc.
    Date Received
    September 29, 1993
    Decision Date
    July 28, 1994
    Product Code
    EAQ
    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
    EAQ Detector, Ultraviolet

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (EAQ), ordered by most recent decision date.

    LIGHT, EXAMINING, DENTAL, ULTRA VIOLET

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    FDA Class 2 ·Dental
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