FDA 510(k) Applications Submitted by MARGARET J LARSON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K981028 |
03/19/1998 |
ULTRA IMAGE AND ULTRA SCAN |
SONOTECH, INC. |
| K031222 |
04/17/2003 |
SCANLUBE |
SONOTECH, INC. |
| K961692 |
05/01/1996 |
SONOSCAN |
SONOTECH, INC. |
| K962093 |
05/29/1996 |
ULTRAMIX |
SONOTECH, INC. |
| K031894 |
06/19/2003 |
SCANTEC PAD |
SONOTECH, INC. |
| K013170 |
09/24/2001 |
SCANTAC MEMBRANE OR SCANTAC STRIP |
SONOTECH, INC. |
| K042619 |
09/24/2004 |
ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT |
SONOTECH, INC. |
| K033178 |
10/01/2003 |
ULTRABIO |
SONOTECH, INC. |
| K983691 |
10/20/1998 |
SCANFLEX SOLID COUPLANT MEMBRANE |
SONOTECH, INC. |
| K013701 |
11/08/2001 |
ENDO-GLIDE |
SONOTECH, INC. |
| K983985 |
11/09/1998 |
HYBRISONIC SHEATH |
SONOTECH, INC. |
| K964658 |
11/20/1996 |
OASIS |
SONOTECH, INC. |
| K984562 |
12/23/1998 |
VIVOSONIC |
SONOTECH, INC. |
|
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