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

    EUSOL-C

    K Number: K032422 · Decision Dec 15, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    20
    Applicant Total
    2
    Review Days
    132

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    Basic Information

    Device Name
    EUSOL-C
    K Number
    K032422
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Al.Chi.Mi.A
    Date Received
    August 5, 2003
    Decision Date
    December 15, 2003
    Product Code
    LYX
    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
    LYX Media, Corneal Storage

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    Other Clearances by Al.Chi.Mi.A

    K Number Device Name
    K063617 EUSOL-C