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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 K792522
Device Name MODEL 980D TENS NEUROPACER
Applicant
Empi
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Empi
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received12/06/1979
Decision Date 12/13/1979
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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