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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 K884869
Device Name MODIFIED MRL NEUROPROBE SYSTEM V
Applicant
Medical Research Laboratories, Inc.
6457 W. Howard St.
Niles,  IL  60648
Applicant Contact DILIP MEHTA
Correspondent
Medical Research Laboratories, Inc.
6457 W. Howard St.
Niles,  IL  60648
Correspondent Contact DILIP MEHTA
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received11/21/1988
Decision Date 06/06/1989
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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