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

    NON-STERILE BROVIAC PARENTERAL ALIMI-

    K Number: K830256 · Decision Mar 1, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    90
    Registration Numbers
    90
    Same Product Code
    301
    Applicant Total
    6
    Review Days
    35

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    Basic Information

    Device Name
    NON-STERILE BROVIAC PARENTERAL ALIMI-
    K Number
    K830256
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5970
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Evermed, Inc.
    Date Received
    January 25, 1983
    Decision Date
    March 1, 1983
    Product Code
    LJS
    Advisory Committee
    General Hospital
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

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    Other Clearances by Evermed, Inc.

    K Number Device Name
    K840846 STERILE HICHMAN/BROVIAC INJECTION CAP
    K840529 STEIGER TUNNELING INSTRUMENT 285
    K830406 NON-STERILE CATHETER REPAIR KITS
    K830233 NON-STERILE,SINGLE/SOUBLE LUMEN-CATH
    K830257 NON-STERILE PERITONEAL ACCESS CATHET-