Ness-Neuromuscular Electrical Stimulation Systems
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K111767 | NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT | GZI | 2011-09-15 | View |
| 510(k) | K080219 | MODIFICATION TO:NESS L300 | GZI | 2008-02-28 | View |
| 510(k) | K053468 | NESS L300 | GZI | 2006-07-07 | View |
| 510(k) | K031900 | HANDMASTER | GZI | 2003-08-08 | View |
| 510(k) | K024279 | NESS CHILDREN SYSTEM | IPG | 2003-02-05 | View |
| 510(k) | K022776 | NESS SYSTEM | IPF | 2002-09-11 | View |
| 510(k) | K012823 | MODIFICATION TO HANDMASTER | GZI | 2001-11-14 | View |
No matching devices.
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