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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