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U.S. Department of Health and Human Services

510(K) Premarket Notification

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Device Name
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Applicant
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510(K)
Number
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Decision
Date
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pro walker pl-200 power wheelchair PRO WALKER INC. k041336 07/20/2004
second look viewer ICAD INC. k042697 11/19/2004
metrx workstation MEDICAL METRX SOLUTIONS, INC. k043134 12/13/2004
modification to verte-stack spinal system MEDTRONIC SOFAMOR DANEK k043566 01/07/2005
14f dual floating dialysis catheter/tray CARDIOMED SUPPLIES, INC. k042672 03/23/2005
diasorin liaison ebna igg, liaison vca igg, liaison vca igm assays DIASORIN, INC. k040120 04/29/2005
tri-ostetic BERKELEY ADVANCED BIOMATERIALS, INC. k041889 08/19/2004
modification to hp m2376a device link system, model m2376a AGILENT TECHNOLOGIES, INC. k001776 06/30/2000
smartwave ms 2000 NEWWAVE MEDICAL LLC k041063 12/01/2004
quickie interchange fwd w/lift power wheelchair SUNRISE MEDICAL k043435 02/11/2005

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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