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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name powered light based laser non-thermal instrument with non-heating effect for adjunctive use in pain therapy
510(k) Number K212189
Device Name FibroLux
Multi Radiance Medical
6521 Davis Industrial Parkway
Solon,  OH  44139
Applicant Contact Andrey Godes
Regulatory Insight, Inc.
33 Golden Eagle Lane
Littleton,  CO  80127
Correspondent Contact Kevin Walls
Regulation Number890.5500
Classification Product Code
Date Received07/13/2021
Decision Date 09/02/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No