510(k) K111767 ยท GZI Stimulator, Neuromuscular, External Functional
NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT
| Applicant | Ness-Neuromuscular Electrical Stimulation Systems, Ra'Anana, IL |
| Decision | Substantially Equivalent, Sep 15, 2011 |
| Received | Jun 23, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111767
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.