Suntech Medical, Inc. is one of 4831 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Suntech Medical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Suntech Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Historical record: 7 cleared submissions from 2005 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Suntech Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Suntech Medical, Inc.
7 devices
Cleared
Feb 19, 2016
Oscar 2
Cardiovascular
259d
Cleared
Nov 02, 2012
TANGO M2 BLOOD PRESSURE MONITOR
Cardiovascular
87d
Cleared
Oct 20, 2008
DISPOSABLE BLOOD PRESSURE CUFF, MODEL DC100
Cardiovascular
207d
Cleared
May 02, 2007
247 BP DEVICE
Cardiovascular
44d
Cleared
Jun 07, 2006
CYCLE BP MONITOR AND PULSE OXIMETER, MODEL 1060
Cardiovascular
72d
Cleared
Jan 05, 2006
TANGO+ AUTOMATIC BLOOD PRESSURE AND OXYGEN SATURATION MEASUREMENT SYSTEM
Cardiovascular
50d
Cleared
Sep 09, 2005
ALL PURPOSE CUFF, MODEL 222APC
Cardiovascular
58d