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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 K951969
Device Name MYOEXORCISER II FUAL
Applicant
VERIMED HOLDINGS, INC.
11950 N.W. 39TH ST., SUITE D
CORAL SPRINGS,  FL  33065
Applicant Contact CHRISTOPHER J CHASE
Correspondent
VERIMED HOLDINGS, INC.
11950 N.W. 39TH ST., SUITE D
CORAL SPRINGS,  FL  33065
Correspondent Contact CHRISTOPHER J CHASE
Regulation Number882.5050
Classification Product Code
HCC  
Date Received04/27/1995
Decision Date 06/14/1995
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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