FDA 510(k) Applications Submitted by DAINA L GRAHAM

FDA 510(k) Number Submission Date Device Name Applicant
K071134 04/23/2007 SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM SONOSITE,INC.
K092058 07/08/2009 SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM SONOSITE,INC.
K052109 08/04/2005 SONOSITE HAND-CARRIED ULTRASOUND SYSTEM (C1 SERIES) SONOSITE,INC.
K053069 11/01/2005 SONOSITE MICROMAXX DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES) SONOSITE,INC.
K043452 12/15/2004 TITAN HIGH RESOLUTION ULTRASOUND SYSTEM AND SONOSITE ULTRASOUND SYSTEM SONOSITE,INC.
K043559 12/27/2004 SONOSITE HIGH-RESOLUTION DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES) SONOSITE,INC.


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