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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name device, biofeedback
510(k) Number K892649
Device Name VERIMED MYOEXORCISER III (MYO III)
Applicant
VERIMED HOLDINGS, INC.
1001 N.W. 62ND STREET, SUITE
212
FORT LAUDERDALE,  FL  33309
Applicant Contact WILLIAM MEE
Correspondent
VERIMED HOLDINGS, INC.
1001 N.W. 62ND STREET, SUITE
212
FORT LAUDERDALE,  FL  33309
Correspondent Contact WILLIAM MEE
Regulation Number882.5050
Classification Product Code
HCC  
Date Received04/12/1989
Decision Date 12/13/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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