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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Muscle, Powered
510(k) Number K893220
Device Name VERIMED MYOEXORCISER VERISTIM
Applicant
Verimed Holdings, Inc.
1001 NW 62nd St., Suite
212
Fort Lauderdale,  FL  33309
Applicant Contact WILLIAM MEE
Correspondent
Verimed Holdings, Inc.
1001 NW 62nd St., Suite
212
Fort Lauderdale,  FL  33309
Correspondent Contact WILLIAM MEE
Regulation Number890.5850
Classification Product Code
IPF  
Date Received04/27/1989
Decision Date 03/07/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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