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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Test, Blood Glucose, Over The Counter
510(k) Number K090609
Device Name OKMETER MATCH BLOOD GLUCOSE MONITORING SYSTEM
Applicant
Ok Biotech Co., Ltd.
# 58, Fu-Chiun St.
Hsin-Chu City,  TW 30067
Applicant Contact Ke-Min Jen
Correspondent
Ok Biotech Co., Ltd.
# 58, Fu-Chiun St.
Hsin-Chu City,  TW 30067
Correspondent Contact Ke-Min Jen
Regulation Number862.1345
Classification Product Code
NBW  
Subsequent Product Codes
CGA   JJX  
Date Received03/06/2009
Decision Date 02/04/2010
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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