Nihon Seimitsu Sokki Co., Ltd. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nihon Seimitsu Sokki Co., Ltd. Cardiovascular ✕
19 devices
Cleared
Aug 02, 2012
DISITAL BLOOD PRESSURE MONITOR
Cardiovascular
329d
Cleared
Feb 24, 2012
BLOOD PRESSURE MONITOR
Cardiovascular
162d
Cleared
Feb 24, 2012
BLOOD PRESSURE MONITOR
Cardiovascular
162d
Cleared
Jun 03, 2010
AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270
Cardiovascular
245d
Cleared
May 09, 2008
WRIST BLOOD PRESSURE MONITOR, MODEL WS-1100/WS-1100PV
Cardiovascular
106d
Cleared
Oct 09, 2007
MODIFICATION TO: DIGITAL BLOOD PRESSURE MONITOR, MODEL 1901
Cardiovascular
145d
Cleared
Aug 10, 2006
DM-3000 DIGITAL BLOOD PRESSURE MONITOR
Cardiovascular
114d
Cleared
Mar 25, 2005
MODEL DS-1901 DIGITAL BLOOD PRESSURE MONITOR
Cardiovascular
7d
Cleared
Feb 24, 2004
DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-1862
Cardiovascular
15d
Cleared
Jul 20, 2001
BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110
Cardiovascular
7d
Cleared
Nov 21, 2000
MODEL WS-500 DIGITAL WRIST BLOOD PRESSURE MONITOR
Cardiovascular
15d
Cleared
Dec 01, 1999
DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181
Cardiovascular
15d