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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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