Mtre Advanced Technology , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mtre Advanced Technology , Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Mtre Advanced Technology , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Mccordsville, US.
Historical record: 6 cleared submissions from 2000 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mtre Advanced Technology , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mtre Advanced Technology , Ltd.
6 devices
Cleared
Nov 18, 2010
CRITICOOL PRO
Cardiovascular
113d
Cleared
Mar 26, 2009
CRITICOOL
Cardiovascular
106d
Cleared
Feb 10, 2003
ALLON 2001 VERSION 5
Cardiovascular
56d
Cleared
Nov 13, 2000
ALLON 2001 MODIFIED
Cardiovascular
18d
Cleared
Jun 08, 2000
ALLON 2001
Cardiovascular
21d
Cleared
Mar 07, 2000
ALLON 2000
Cardiovascular
235d