Suntech Medical Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Suntech Medical Instruments, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Suntech Medical Instruments, Inc. has 5 FDA 510(k) cleared medical devices. Based in Raleigh, US.
Historical record: 5 cleared submissions from 1992 to 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Suntech Medical Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Suntech Medical Instruments, Inc.
5 devices
Cleared
Mar 29, 2001
PRESSURE TRAK, MODEL 222-B
Cardiovascular
27d
Cleared
Oct 25, 2000
OSCAR 2, MODEL 222
Cardiovascular
30d
Cleared
Jan 02, 1998
TANGO NON-INVASIVE BLOOD PRESSURE MONITOR
Cardiovascular
317d
Cleared
Sep 04, 1992
4240 DYNAMIC BP/HEART RATE MONITOR
Cardiovascular
347d
Cleared
Jul 14, 1992
ACCUTRACKER DX
Cardiovascular
321d