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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 K843822
Device Name MEA110
Applicant
CANADIAN MEDICAL PRODUCTS
18 KENSINGTON ROAD
SUITE 203
BRAMALEA ONTARIO,  CA
Applicant Contact ALAN L RUSSELL
Correspondent
CANADIAN MEDICAL PRODUCTS
18 KENSINGTON ROAD
SUITE 203
BRAMALEA ONTARIO,  CA
Correspondent Contact ALAN L RUSSELL
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received09/28/1984
Decision Date 10/22/1984
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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