Nihon Seimitsu Sokki Co., Ltd. is one of 122 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Nihon Seimitsu Sokki Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DISITAL BLOOD PRESSURE MONITOR, BLOOD PRESSURE MONITOR, BLOOD PRESSURE MONITOR
21
Total
21
Cleared
0
Denied
Nihon Seimitsu Sokki Co., Ltd. has 21 FDA 510(k) cleared cardiovascular devices. Based in Shibukawa-Shi, Gunma-Ken, JP.
Historical record: 21 cleared submissions from 1985 to 2012.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv Product Service, Inc. and Kema Quality B.V..
FDA 510(k) Regulatory Record - Nihon Seimitsu Sokki Co., Ltd.
21 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
Feb 15, 2008
POTABLE AIR MASSAGER PUTIFINO, MODEL AM-7
Physical Medicine
248d
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
Aug 01, 2003
WRIST BLOOD PRESSURE MONITOR & FAT METER, MODEL WT-20
Gastroenterology & Urology
72d
Cleared
Jul 20, 2001
BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110
Cardiovascular
7d