Echosens
Echosens holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2023.
Top product codes for Echosens
Recent clearances by Echosens
- K223902 — FibroScan® device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630)
- K212035 — FibroScan 230
- K203273 — FibroScan® Family of Products (Models: 502 Touch, 530 Compact, 430 Mini+, and 630)
- K200655 — FibroScan® 630
- K181547 — FibroScan® Family of Products (Models: 502 Touch, 530 Compact, and 430 Mini+)
- K173034 — FibroScan® Family of Products (Models: 502 Touch, 530 Compact, and 430 Mini+)
- K172142 — FibroScan 430 Mini+
- K160524 — FibroScan 530 Compact
- K150239 — FibroScan
- K150949 — FibroScan
- K123806 — FIBROSCAN
Data sourced from openFDA. This site is unofficial and independent of the FDA.