Fukuda Denshi USA, Inc. - FDA 510(k) Cleared Devices
68
Total
68
Cleared
0
Denied
Fukuda Denshi USA, Inc. has 68 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 68 cleared submissions from 1984 to 2018.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
68 devices
Cleared
Apr 16, 2018
CardiMax Electrocardiograph
Cardiovascular
195d
Cleared
Mar 16, 2015
Fukuda Denshi DynaScope Model DS-8000 Series Patient Monitor
Cardiovascular
67d
Cleared
Feb 12, 2015
FUKUDA DENSHI DYNASCOPE MODEL DS-8100N/8100M PATIENT MONITOR
Cardiovascular
408d
Cleared
Dec 21, 2011
FUKUDA DENSHI VASERA MODEL VS-1500
Cardiovascular
112d
Cleared
Mar 11, 2011
FUKUDA DENSHI
Cardiovascular
137d
Cleared
Mar 19, 2009
FUKUDA DENSHI DYNASCOPE MODEL DS-7000 SERIES PATIENT MONITOR, MODEL...
Cardiovascular
94d
Cleared
Sep 30, 2008
MODEL FF SONIC US-750 XT DIAGNOSTIC ULTRASOUND SYSTEM 3D IMAGING UNIT
Radiology
18d
Cleared
Aug 29, 2008
FUKUDA DENSHI DYNASCOPE MODEL DS-7000/7000M PATIENT MONITOR
Cardiovascular
58d
Cleared
Feb 17, 2005
FUKUDA DENSHI MODEL UF-850XTD
Radiology
3d
Cleared
Jun 03, 2004
FUKUDA DENSHI DYNASCOPE MODEL DS-5000 CENTRAL TELEMETRY SYSTEM
Cardiovascular
190d
Cleared
May 26, 2004
FUKUDA DENSHI DYNASCOPE MODEL DS-7141 PORTABLE PATIENT MONITOR
Cardiovascular
113d
Cleared
Oct 31, 2003
FUKUDA DENSHI MODEL FF SONIC UF-750XT
Radiology
28d
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