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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Imaging, Pulsed Echo, Ultrasonic
510(k) Number K223902
Device Name FibroScan® device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630)
Applicant
Echosens
6 Rue Ferrus
Paris,  FR 75014
Applicant Contact Fanny Patoureaux
Correspondent
Boston Medtech Advisors, Inc.
990 Washington St., Suite 204
Dedham,  MA  02026
Correspondent Contact Zvi Ladin
Regulation Number892.1560
Classification Product Code
IYO  
Subsequent Product Code
ITX  
Date Received12/28/2022
Decision Date 03/02/2023
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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