FDA 510(k) Applications Submitted by Jordan Lydia Grimmer
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| 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. |
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