Ness-Neuromuscular Electrical Stimulation Systems - FDA 510(k) Cleare...
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ness-Neuromuscular Electrical Stimulation Systems Neurology ✕
5 devices
Cleared
Sep 15, 2011
NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT
Neurology
84d
Cleared
Feb 28, 2008
MODIFICATION TO:NESS L300
Neurology
30d
Cleared
Jul 07, 2006
NESS L300
Neurology
206d
Cleared
Aug 08, 2003
HANDMASTER
Neurology
50d
Cleared
Nov 14, 2001
MODIFICATION TO HANDMASTER
Neurology
90d