Agamatrix is one of 16298 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Agamatrix - FDA 510(k) Cleared Devices
Recent clearances: WaveSense Jazz Blood Glucose Monitoring System, WAVESENSE DIABETES MANAGER MODEL VERSION 1.3.4, WAVESENSE KEYNOTE CODELESS BLOOD GLUCOSE MONITORING SYSTEM
7
Total
7
Cleared
0
Denied
Agamatrix has 7 FDA 510(k) cleared medical devices. Based in Salem, US.
Latest FDA clearance: Jun 2024. Active since 2006. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Agamatrix Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Agamatrix
7 devices
Cleared
Jun 06, 2024
WaveSense Jazz Blood Glucose Monitoring System
Chemistry
28d
Cleared
Oct 18, 2010
WAVESENSE DIABETES MANAGER MODEL VERSION 1.3.4
Chemistry
132d
Cleared
Jan 30, 2008
WAVESENSE KEYNOTE CODELESS BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
41d
Cleared
Sep 27, 2007
MODIFICATION TO: JAZZ BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
30d
Cleared
Jul 20, 2007
JAZZ BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
60d
Cleared
Jan 12, 2007
LIBERTY BLOOD GLUCOSE MONITORING SYSTEM, MODEL 8000-0067
Chemistry
60d
Cleared
Nov 13, 2006
ZERO-CLICK DATA MANAGEMENT SYSTEM, MODEL 8000-01528
Chemistry
84d