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

    ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set

    K Number: K153652 · Decision Jun 21, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    81
    Registration Numbers
    81
    Same Product Code
    154
    Applicant Total
    10
    Review Days
    183

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    Basic Information

    Device Name
    ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set
    K Number
    K153652
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5140
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Teleflex, Inc.
    Date Received
    December 21, 2015
    Decision Date
    June 21, 2016
    Product Code
    CAZ
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CAZ Anesthesia Conduction Kit

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    Other Clearances by Teleflex, Inc.

    K Number Device Name
    K140110 FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET
    K141940 CONCHASMART COLUMN
    K140556 CONCHASMART BREATHING CIRCUIT
    K131912 CONCHATHERM NEPTUNE HEATED HUMIDIFIER, COMFORT FLO HUMIDIFICATION SYSTEM, CONCHASMART COLUMN
    K123974 PERCUTANEOUS INTRODUCER KIT
    K121403 CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET
    K103658 FLEXTIP PLUS CLOSED TIP EPIDURAL CATHERTER
    K861951 MODIFIED TELEFLEX MEDICAL INTRODUCER CATHETER
    K860307 PEEL AWAY & SPLIT SHEATH PERCU CATH INTRODUCER SET