510(k) K051178 ยท GWF Stimulator, Electrical, Evoked Response
MEE-1000A NEUROMASTER
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Aug 17, 2005 |
| Received | May 9, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051178
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 17, 2016 | Nihon Kohden America Inc MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stimulator Box) JB-116B, JB-132B (Amplifiers) Electromyography. (EMG) Terminated |
GWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.