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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 K032653
Device Name E275
Applicant
MICRO CURRENT TECHNOLOGY, INC.
4822 CALIFORNIA AVE., S.W.,
SUITE 201
SEATTLE,  WA  98116
Applicant Contact DAVID SUZUKI
Correspondent
UNDERWRITERS LABORATORIES, INC.
2600 NW LAKE RD.
CAMAS,  WA  98607 -9526
Correspondent Contact MARC M MOUSER
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received08/28/2003
Decision Date 09/12/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Statement Statement
Type Traditional
Reviewed by Third Party Yes
Combination Product No
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