Echosens
11 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| FibroScan® device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630) (K223902) | Echosens | 2023-03-02 |
| FibroScan 230 (K212035) | Echosens | 2021-07-30 |
| FibroScan® Family of Products (Models: 502 Touch, 530 Compact, 430 Mini+, and 630) (K203273) | Echosens | 2021-03-25 |
| FibroScan® 630 (K200655) | Echosens | 2020-07-16 |
| FibroScan® Family of Products (Models: 502 Touch, 530 Compact, and 430 Mini+) (K181547) | Echosens | 2018-07-09 |
| FibroScan® Family of Products (Models: 502 Touch, 530 Compact, and 430 Mini+) (K173034) | Echosens | 2017-11-14 |
| FibroScan 430 Mini+ (K172142) | Echosens | 2017-09-13 |
| FibroScan 530 Compact (K160524) | Echosens | 2016-03-18 |
| FibroScan (K150239) | Echosens | 2015-09-01 |
| FibroScan (K150949) | Echosens | 2015-06-03 |
| FIBROSCAN (K123806) | Echosens | 2013-04-05 |
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Every clearance here is in the API, with alerts when new ones post.