FDA 510(k) Applications Submitted by ECHOSENS
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K150239 |
02/02/2015 |
FibroScan |
Echosens |
| K150949 |
04/08/2015 |
FibroScan |
ECHOSENS |
| K223902 |
12/28/2022 |
FibroScan« device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630) |
Echosens |
| K160524 |
02/25/2016 |
FibroScan 530 Compact |
ECHOSENS |
| K200655 |
03/12/2020 |
FibroScan« 630 |
Echosens |
| K181547 |
06/12/2018 |
FibroScan« Family of Products (Models: 502 Touch, 530 Compact, and 430 Mini+) |
Echosens |
| K212035 |
06/30/2021 |
FibroScan 230 |
Echosens |
| K172142 |
07/17/2017 |
FibroScan 430 Mini+ |
Echosens |
| K173034 |
09/28/2017 |
FibroScan« Family of Products (Models: 502 Touch, 530 Compact, and 430 Mini+) |
Echosens |
| K203273 |
11/06/2020 |
FibroScan« Family of Products (Models: 502 Touch, 530 Compact, 430 Mini+, and 630) |
Echosens |
| K123806 |
12/10/2012 |
FIBROSCAN |
ECHOSENS |
|
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