BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    LAS-2 ALIGNMENT SYSTEM

    K Number: K834538 · Decision Feb 21, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35
    Same Product Code
    122
    Applicant Total
    2
    Review Days
    71

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    Basic Information

    Device Name
    LAS-2 ALIGNMENT SYSTEM
    K Number
    K834538
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5820
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Therados, Inc.
    Date Received
    December 12, 1983
    Decision Date
    February 21, 1984
    Product Code
    KPO
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KPO Dialysate Concentrate For Hemodialysis (Liquid Or Powder)

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    Other Clearances by Therados, Inc.

    K Number Device Name
    K834201 TCT-1 TREATMENT COUCH