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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Nerve, Transcutaneous, For Pain Relief
510(k) Number K844680
Device Name CYBERTENS
Applicant
PORI ASSOCIATES, INC.
1825 PALMETTO AVE.
DACIFICA,  CA  94044
Applicant Contact JOHN PORI
Correspondent
PORI ASSOCIATES, INC.
1825 PALMETTO AVE.
DACIFICA,  CA  94044
Correspondent Contact JOHN PORI
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received11/30/1984
Decision Date 04/05/1985
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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