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

    LEE SYRINGE

    K Number: K842371 · Decision Jan 14, 1985
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    213

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    Basic Information

    Device Name
    LEE SYRINGE
    K Number
    K842371
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Peter F. Lee, Inc.
    Date Received
    June 15, 1984
    Decision Date
    January 14, 1985
    Advisory Committee
    Unknown
    Review Advisory Committee
    DE
    Third Party
    N