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

    SUN BED BY VERRE ET QUARTZ UVA-FRANCE

    K Number: K833229 · Decision Jan 27, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    1
    Applicant Total
    1
    Review Days
    156

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    SUN BED BY VERRE ET QUARTZ UVA-FRANCE
    K Number
    K833229
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.4445
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    H & M Douglas Enterprises, Inc.
    Date Received
    August 24, 1983
    Decision Date
    January 27, 1984
    Product Code
    FTZ
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FTZ Locator, Magnetic

    Similar 510(k) Clearances

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

    MODEL 200

    FDA 510(k)
    FDA Class 1 ·Ophthalmic
    View all