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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 K933368
Device Name TENS-IT
Applicant
Electro Med Supply, Inc.
P.O. Drawer 179
19207 Jayhawk Dr.
Penn Valley,  CA  95946
Applicant Contact THOMAS V DAIGLE
Correspondent
Electro Med Supply, Inc.
P.O. Drawer 179
19207 Jayhawk Dr.
Penn Valley,  CA  95946
Correspondent Contact THOMAS V DAIGLE
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received07/09/1993
Decision Date 06/07/1994
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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