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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 K152365
Device Name AgaMatrix Jazz Wireless 2 Blood Glucose Monitoring System
AgaMatrix, Inc.
7C Raymond Avenue
Salem,  NH  03079
Applicant Contact David Olsen
AgaMatrix, Inc.
7C Raymond Avenue
Salem,  NH  03079
Correspondent Contact David Olsen
Regulation Number862.1345
Classification Product Code
Subsequent Product Code
Date Received08/21/2015
Decision Date 04/21/2016
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