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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Acupressure
510(k) Number K900588
Device Name ACU-BAND ACCUPRESSURE WRIST BAND
Applicant
Euro-Am Pharma, Inc.
64 Montrose Ave.
Fanwood,  NJ  07023
Applicant Contact GYAN, PHD
Correspondent
Euro-Am Pharma, Inc.
64 Montrose Ave.
Fanwood,  NJ  07023
Correspondent Contact GYAN, PHD
Classification Product Code
MVV  
Date Received02/07/1990
Decision Date 02/22/1990
Decision Substantially Equivalent (SESE)
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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