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

    PROCEDURE READY TRAYS

    K Number: K884577 · Decision Aug 1, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    205
    Same Product Code
    503
    Applicant Total
    19
    Review Days
    273

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    Basic Information

    Device Name
    PROCEDURE READY TRAYS
    K Number
    K884577
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Applicant
    Professional Medical Services
    Date Received
    November 1, 1988
    Decision Date
    August 1, 1989
    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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    K904954 CONDOR DIGITAL INFLATION SYRINGE
    K902606 RADIOPAQUE RULER
    K890471 PMS ANGIO DRAPE
    K884497 CONTROL SYRINGE
    K872448 BLOOD CONTAINMENT PACK
    K864555 3 RING ATTACHMENT
    K854941 PMS PERCUTANEOUS PUNCTURE NEEDLE
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