Medical Device Manufacturer · CN , Hong Kong

Fuji Dynamics Limited - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2000

Recent clearances: INF 4160 PLUS, MODEL D-FJ31F, FD EMS, MODEL # D-FJ30E, FD TENS 2030, MODEL DFJ24T

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Fuji Dynamics Limited Neurology ✕

6 devices

1-6 of 6

Cleared Jan 07, 2010

INF 4160 PLUS, MODEL D-FJ31F

Neurology · 119d

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

Neurology · 17d

Cleared Jul 06, 2000

MEDISANA DIGITAL TENS

Neurology · 202d

Cleared Jul 06, 2000

Neurology · 202d