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

    VAS-CATH PERITONEAL DIALYSIS CATHETER

    K Number: K871817 · Decision Jul 16, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    26
    Registration Numbers
    26
    Same Product Code
    47
    Applicant Total
    19
    Review Days
    66

    Basic Information

    Device Name
    VAS-CATH PERITONEAL DIALYSIS CATHETER
    K Number
    K871817
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5630
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    VAS-CATH OF CANADA LTD.
    Date Received
    May 11, 1987
    Decision Date
    July 16, 1987
    Product Code
    FJS
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FJS Catheter, Peritoneal, Long-Term Indwelling

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    Other Clearances by VAS-CATH OF CANADA LTD.

    K Number Device Name
    K875188 LUER LOCK CONNECTORS / RIDIG P.V.C.
    K871488 VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATH
    K871487 VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATH
    K863982 VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY
    K853283 VACCESS TM 4006
    K844854 OPTI-FLOW DIGITAL SUBTRACTION ANGIOGRAPHY CAT-KIT
    K844800 OPTI-FLOW & OPTI-TORQUE ANGIOGRAPHIC CATHETERS
    K850009 EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER
    K844433 VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA
    K844336 VAS-CATH PARALLEL DUAL LUMAN JUGULAR CANNUAL CATH
    Search all 19 clearances from VAS-CATH OF CANADA LTD. →