Company ยท US
Ness-Neuromuscular Electrical Stimulation Systems
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2011. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 15, 2011 | K111767 | NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT Ness-Neuromuscular Electrical Stimulation Systems, IL | GZI |
| Feb 28, 2008 | K080219 | MODIFICATION TO:NESS L300 Ness-Neuromuscular Electrical Stimulation Systems | GZI |
| Jul 7, 2006 | K053468 | NESS L300 Ness-Neuromuscular Electrical Stimulation Systems | GZI |
| Aug 8, 2003 | K031900 | HANDMASTER Ness-Neuromuscular Electrical Stimulation Systems | GZI |
| Feb 5, 2003 | K024279 | NESS CHILDREN SYSTEM Ness-Neuromuscular Electrical Stimulation Systems | IPG |
| Sep 11, 2002 | K022776 | NESS SYSTEM Ness-Neuromuscular Electrical Stimulation Systems | IPF |
| Nov 14, 2001 | K012823 | MODIFICATION TO HANDMASTER Ness-Neuromuscular Electrical Stimulation Systems | GZI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||