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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Dynamometer, Ac-Powered
510(k) Number K922029
Device Name REMUSK MP
Applicant
Equipement Biomedical Specialise, Inc.
2155 Guy St.
#820, Montreal
Canada,  CA H3H 2R9
Applicant Contact SYLVAIN BOUCHER
Correspondent
Equipement Biomedical Specialise, Inc.
2155 Guy St.
#820, Montreal
Canada,  CA H3H 2R9
Correspondent Contact SYLVAIN BOUCHER
Regulation Number888.1240
Classification Product Code
LBB  
Date Received05/01/1992
Decision Date 10/06/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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