Ness-Neuromuscular Electrical Stimulation Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ness-Neuromuscular Electrical Stimulation Systems - FDA 510(k) Cleare...
7
Total
7
Cleared
0
Denied
Ness-Neuromuscular Electrical Stimulation Systems has 7 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 7 cleared submissions from 2001 to 2011. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ness-Neuromuscular Electrical Stimulation Systems Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ness-Neuromuscular Electrical Stimulation Systems
7 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
Feb 05, 2003
NESS CHILDREN SYSTEM
Physical Medicine
44d
Cleared
Sep 11, 2002
NESS SYSTEM
Physical Medicine
21d
Cleared
Nov 14, 2001
MODIFICATION TO HANDMASTER
Neurology
90d