Ness-Neuromuscular Electrical Stimulation Systems
Ness-Neuromuscular Electrical Stimulation Systems appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 15, 2011.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K111767 | NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT | September 15, 2011 |
| K080219 | MODIFICATION TO:NESS L300 | February 28, 2008 |
| K053468 | NESS L300 | July 7, 2006 |
| K031900 | HANDMASTER | August 8, 2003 |
| K024279 | NESS CHILDREN SYSTEM | February 5, 2003 |
| K022776 | NESS SYSTEM | September 11, 2002 |
| K012823 | MODIFICATION TO HANDMASTER | November 14, 2001 |