FDA 510(k) Applications Submitted by FUJIFILM SONOSITE, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K183235 |
11/20/2018 |
SonoSite SII Ultrasound System |
FUJIFILM SonoSite, Inc. |
| K190476 |
02/27/2019 |
FUJIFILM Sonosite Vevo MD Imaging System |
FUJIFILM SonoSite, Inc. |
| K213763 |
12/01/2021 |
Sonosite PX Ultrasound System |
FUJIFILM Sonosite, Inc. |
| K162045 |
07/25/2016 |
SonoSite SII Ultrasound System, SonoSite Edge II Ultrasound System |
FUJIFILM SonoSite, Inc. |
| K171437 |
05/16/2017 |
SonoSite X-Porte Ultrasound System |
FujiFilm SonoSite, Inc. |
| K160734 |
03/17/2016 |
SonoSite SII Ultrasound System |
FUJIFILM SonoSite, Inc. |
| K142017 |
07/25/2014 |
X-PORTE ULTRASOUND SYSTEM |
FUJIFILM SonoSite, Inc. |
| K162288 |
08/15/2016 |
SonoSite iViz Ultrasound System |
FUJIFILM SONOSITE, INC. |
| K160406 |
02/16/2016 |
FUJIFILM FC1 Ultrasound System |
FUJIFILM SonoSite, Inc. |
| K160674 |
03/10/2016 |
Fujifilm Sonosite Vevo MD Imaging System |
FUJIFILM SONOSITE, INC. |
| K180704 |
03/19/2018 |
SonoSite iViz Ultrasound System |
FUJIFILM SonoSite, Inc. |
| K200964 |
04/10/2020 |
Sonosite PX Ultrasound System |
FUJIFILM SonoSite, Inc. |
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