Fasstech - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Fasstech has 9 FDA 510(k) cleared medical devices. Based in Burlington, US.
Historical record: 9 cleared submissions from 1993 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Fasstech Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Fasstech
9 devices
Cleared
Aug 16, 2007
INSIGHT DISCOVERY
Neurology
274d
Cleared
Nov 28, 2003
CWAS 1000
Neurology
29d
Cleared
Oct 10, 2003
INSIGHT MILLENNIUM III
Neurology
379d
Cleared
Sep 20, 2001
INSIGHT MILLENNIUM PLUS
Neurology
87d
Cleared
Aug 30, 2001
INSIGHT GENESIS
Neurology
65d
Cleared
Jun 03, 1999
INSIGHT MILLENNIUM
Neurology
86d
Cleared
Jun 12, 1996
SPINAL TOUCH
Neurology
76d
Cleared
Feb 24, 1995
FOCUS EMG
Neurology
415d
Cleared
Feb 02, 1993
PSI 220 DUAL EMG
Neurology
110d