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

    I.V. START KIT

    K Number: K932071 · Decision Feb 17, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    205
    Same Product Code
    503
    Applicant Total
    16
    Review Days
    295

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    Basic Information

    Device Name
    I.V. START KIT
    K Number
    K932071
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Clinipad Corp.
    Date Received
    April 28, 1993
    Decision Date
    February 17, 1994
    Product Code
    FOZ
    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
    FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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    Other Clearances by Clinipad Corp.

    K Number Device Name
    K931560 CARDIAC CATHETERIZATION TRAY
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    K932010 V.A.D. ACCESS KIT
    K932036 LACERATION TRAY
    K932016 TRACHEOSTOMY CARE TRAY
    K862562 PUNCH BIOPSY KIT
    K862563 TRACHEOSTOMY CLEANSING SOLUTION
    K833075 WET DRESSING KIT
    K833432 CATHETER INSERTION KIT
    K830476 OR PREP KIT
    Search all 16 clearances from Clinipad Corp. →