FDA 510(k) Applications Submitted by MICHAEL HOFFMAN

FDA 510(k) Number Submission Date Device Name Applicant
K030949 03/26/2003 TITAN HIGH RESOLUTION ULTRASOUND SYSTEM SONOSITE,INC.
K014116 12/14/2001 HAND-CARRIED ULTRASOUND SYSTEM SONOSITE,INC.
K030064 01/07/2003 ILOOK 25 NEEDLE GUIDE ATTACHMENT AND BRACKET ASSEMBLY SONOSITE,INC.
K010374 02/07/2001 SONOSITE HAND-CARRIED ULTRASOUND SYSTEM SONOSITE,INC.
K021628 05/17/2002 SONOSITE HAND-CARIED UNTRASOUND SYSTEM (POWERSERIES) SONOSITE,INC.
K112626 09/09/2011 LIPSONIX(R) SYSTEM MODEL 2 MEDICIS TECHNOLOGIES CORPORATION
K033367 10/21/2003 TITAN ULTRASOUND SYSTEM, SONOSITE ILOOK 25 ULTRASOUND SYSTEM, 180PLUS ULTRASOUND SYSTEM, MODEL L03073, L02245, L02464 SONOSITE,INC.
K003399 11/01/2000 SONOSITE HAND-CARRIED ULTRASOUND SYSTEM SONOSITE,INC.
K023957 11/27/2002 SONOSITE HAND-CARRIED ULTRASOUND SYSTEM (C2 SERIES) SONOSITE,INC.
K994096 12/03/1999 SONOHEART HAND-CARRIED ECHOCARDIOGRAPHY SYSTEM SONOSITE,INC.


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