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

    CERNER PROVISION WORKSTATION (VERSION 2.5)

    K Number: K091032 · Decision Jun 22, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    7
    Review Days
    73

    Basic Information

    Device Name
    CERNER PROVISION WORKSTATION (VERSION 2.5)
    K Number
    K091032
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    CERNER CORP.
    Date Received
    April 10, 2009
    Decision Date
    June 22, 2009
    Product Code
    LLZ
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LLZ System, Image Processing, Radiological

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (LLZ), ordered by most recent decision date.

    CustomSurg OrthoPlanner

    FDA 510(k)
    FDA Class 2 ·Radiology

    uOmniscan

    FDA 510(k)
    FDA Class 2 ·Radiology

    Mosaic (V1.0.1)

    FDA 510(k)
    FDA Class 2 ·Radiology

    UroNav 4

    FDA 510(k)
    FDA Class 2 ·Radiology

    TechLive

    FDA 510(k)
    FDA Class 2 ·Radiology

    SMARTDent

    FDA 510(k)
    FDA Class 2 ·Radiology
    View all

    Other Clearances by CERNER CORP.

    K Number Device Name
    K121758 CERNER FETALINK+(VERSION1.0)
    K093134 CERNER CAREAWARE IBUS
    K091251 CERNER FETALINK (VERSION 1.0)
    K070394 CERNER PROVISION WORKSTATION
    K000770 PROVIEW MEDICAL IMAGE DISPLAY MODULE
    K955000 REMOTE VIEWING SYSTEM MEDICAL IMAGE DISPLAY MODULE