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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 K790011
Device Name STIMULATOR, MENTOR 100 NERVE
Applicant
MENTOR CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
MENTOR CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received01/02/1979
Decision Date 03/02/1979
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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