BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

    THERALASE TLC-1000 THERAPEUTIC MEDICAL LASER SYSTEM

    K Number: K050342 · Decision Jul 11, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    20
    Registration Numbers
    20
    Same Product Code
    53
    Applicant Total
    2
    Review Days
    150

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    Basic Information

    Device Name
    THERALASE TLC-1000 THERAPEUTIC MEDICAL LASER SYSTEM
    K Number
    K050342
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5500
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Theralase, Inc.
    Date Received
    February 11, 2005
    Decision Date
    July 11, 2005
    Product Code
    NHN
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    NHN Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy

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    Other Clearances by Theralase, Inc.

    K Number Device Name
    K151816 TLC-2000 Therapeutic Medical Laser System