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

    ALLERGAN LENS CASE

    K Number: K884251 · Decision Dec 28, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    44
    Registration Numbers
    44
    Same Product Code
    81
    Applicant Total
    2
    Review Days
    78

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    Basic Information

    Device Name
    ALLERGAN LENS CASE
    K Number
    K884251
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.5928
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Allergan Optical
    Date Received
    October 11, 1988
    Decision Date
    December 28, 1988
    Product Code
    LRX
    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
    LRX Case, Contact Lens

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    Other Clearances by Allergan Optical

    K Number Device Name
    K881987 DURACLEAN DAILY CLEANER