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

    NIPRO DISPOSABLE SYRINGES

    K Number: K030683 · Decision Oct 31, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    27
    Review Days
    240

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    Basic Information

    Device Name
    NIPRO DISPOSABLE SYRINGES
    K Number
    K030683
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Nipro Medical Corp.
    Date Received
    March 5, 2003
    Decision Date
    October 31, 2003
    Product Code
    FMF
    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
    FMF Syringe, Piston

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    Other Clearances by Nipro Medical Corp.

    K Number Device Name
    K093985 NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLE
    K081210 NIPRO SAFETOUCH HUBER INFUSTION SET
    K072024 NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL A201-A219, V801-V806, 5M9634, 5M9693
    K063368 NIPRO BIOHOLE NEEDLE
    K063721 NIPRO SAFETOUCH II GAMMA
    K052474 NIPRO HYPODERMIC NEEDLE
    K051574 NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE
    K041779 NIPRO DISPOSABLE STOPCOCKS, MODELS 3W-RC. NCN-3, 3W-R, 3W-L
    K032777 MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLE
    K022756 NIPRO BIO-FLEX CATHETER
    Search all 27 clearances from Nipro Medical Corp. →