BEUDAMED
    FDA 510(k) Substantially Equivalent 🇬🇧 United Kingdom

    LENSOMETER

    K Number: K832085 · Decision Aug 16, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    97
    Review Days
    49

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    Basic Information

    Device Name
    LENSOMETER
    K Number
    K832085
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    CooperVision, Inc.
    Date Received
    June 28, 1983
    Decision Date
    August 16, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    OP
    Third Party
    N

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    K213164 Avaira Vitality
    K202756 Clariti 1 Day (somofilcon A), Clariti 1 Day Toric (somofilcon A), Clariti 1 Day Multifocal (somofilcon A), Clariti 1 Day Multifocal Toric (somofilcon A)
    K191763 MyDay (Stenfilcon A) ASPHERE, MyDay (Stenfilcon A) TORIC, MyDay (Stenfilcon A) MULTIFOCAL, MyDay (Stenfilcon A) MULTIFOCAL TORIC
    K190965 MyDay
    K181920 Clariti 1 day (somofilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens with UV Blocker
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