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FDA 510(k) Applications Submitted by KARINE BONENFANT
FDA 510(k) Number
Submission Date
Device Name
Applicant
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
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