Fuji Dynamics Limited is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Fuji Dynamics Limited - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Fuji Dynamics Limited has 7 FDA 510(k) cleared medical devices. Based in Hong Kong, CN.
Historical record: 7 cleared submissions from 2000 to 2010. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Fuji Dynamics Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fuji Dynamics Limited
7 devices
Cleared
Jan 07, 2010
INF 4160 PLUS, MODEL D-FJ31F
Neurology
119d
Cleared
Dec 13, 2007
FD EMS, MODEL # D-FJ30E
Physical Medicine
371d
Cleared
Jan 25, 2006
FD TENS 2030, MODEL DFJ24T
Neurology
113d
Cleared
Feb 11, 2005
INF 4160, MODEL D-FJ27F
Neurology
63d
Cleared
May 20, 2004
L-TENS
Neurology
17d
Cleared
Jul 06, 2000
MEDISANA DIGITAL TENS
Neurology
202d
Cleared
Jul 06, 2000
FDTENS 2010
Neurology
202d