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

    SYRINGE, BLOOD, SAMPLING, ARTERIAL

    K Number: K772338 · Decision Jan 26, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    645
    Review Days
    35

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    Basic Information

    Device Name
    SYRINGE, BLOOD, SAMPLING, ARTERIAL
    K Number
    K772338
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    C.R. Bard, Inc.
    Date Received
    December 22, 1977
    Decision Date
    January 26, 1978
    Product Code
    FMF
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HE
    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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