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

    UltraFlo-R Push Button Blood Collection Set

    K Number: K220458 · Decision Sep 29, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    218
    Registration Numbers
    218
    Same Product Code
    235
    Applicant Total
    6
    Review Days
    589

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    Basic Information

    Device Name
    UltraFlo-R Push Button Blood Collection Set
    K Number
    K220458
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1675
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Innovative Medical Technologies, Inc.
    Date Received
    February 17, 2022
    Decision Date
    September 29, 2023
    Product Code
    JKA
    Advisory Committee
    Clinical Chemistry
    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
    JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

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    K936087 CARPAL BOX
    K904237 RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM
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