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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 K840098
Device Name MODEL 811 VERI/TENS & PO
Applicant
Verite
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Verite
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received01/10/1984
Decision Date 07/17/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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