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

    JMS PLANECTA STOPCOCK

    K Number: K070143 · Decision Apr 10, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    88
    Registration Numbers
    88
    Same Product Code
    88
    Applicant Total
    10
    Review Days
    84

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    Basic Information

    Device Name
    JMS PLANECTA STOPCOCK
    K Number
    K070143
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Jms North America Corp.
    Date Received
    January 16, 2007
    Decision Date
    April 10, 2007
    Product Code
    FMG
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FMG Stopcock, I.V. Set

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    Other Clearances by Jms North America Corp.

    K Number Device Name
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    K082882 A.V. FISTULA BLUNT NEEDLE SET
    K070234 JMS SYSLOC MINI AVF AND APHERESIS NEEDLE SETS
    K051814 JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
    K032975 JMS BLOOD TUBING SETS
    K032977 JMS BYPASS TUBE
    K040247 PLUME SAFETY AVF NEEDLE
    K030479 JMS SYSLOC A.V. FISTULA NEEDLE SET, JMS SYSLOC APHERESIS NEEDLE SET
    K023668 JMS EXTENSION SET WITH PLANECTA, PLANECTA (STAND ALONE UNIT), PLANECTA LOCK & PLANECTA ADAPTOR