Agamatrix, Inc. is one of 4740 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Agamatrix, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Agamatrix, Inc. has 7 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Historical record: 7 cleared submissions from 2006 to 2016. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Agamatrix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Agamatrix, Inc.
7 devices
Cleared
Nov 30, 2016
One Drop Blood Glucose Monitoring System
Chemistry
148d
Cleared
Apr 21, 2016
AgaMatrix Jazz Wireless 2 Blood Glucose Monitoring System
Chemistry
244d
Cleared
Nov 20, 2013
AGAMATRIX HEALTH MANAGER
Chemistry
72d
Cleared
Apr 17, 2013
IBGSTAR BLOOD GLUCOSE MONITORING SYSTEM, IBGSTAR DIABETES MANAGER APPLICATION
Chemistry
47d
Cleared
Dec 07, 2011
IBGSTAR BLOOD GLUCOSE MONITORING SYSTEM, IBGSTAR DIABETES MANAGER...
Chemistry
370d
Cleared
Feb 03, 2009
JAZZ WIRELESS BLOOD GLUCOSE MONITORING SYSTEM, MODEL 8000-03381
Chemistry
90d
Cleared
Jan 23, 2006
LIBERTY BLOOD GLUCOSE MONITORING SYSTEM, MODEL 8000-0067
Chemistry
115d