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

    INFRADIODE INFRARED LAMP

    K Number: K837517 · Decision Jun 14, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    32

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    Basic Information

    Device Name
    INFRADIODE INFRARED LAMP
    K Number
    K837517
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Phimo of Texas, Inc.
    Date Received
    May 13, 1983
    Decision Date
    June 14, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N