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

    CONTACT LENS CLEANSER

    K Number: K780823 · Decision Jun 30, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    73
    Applicant Total
    1
    Review Days
    39

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    Basic Information

    Device Name
    CONTACT LENS CLEANSER
    K Number
    K780823
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Ketchum Laboratories, Inc.
    Date Received
    May 22, 1978
    Decision Date
    June 30, 1978
    Product Code
    HPX
    Advisory Committee
    Unknown
    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
    HPX Lens, Contact (Polymethylmethacrylate)

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