510(k) K012823 ยท GZI Stimulator, Neuromuscular, External Functional
MODIFICATION TO HANDMASTER
| Applicant | Ness-Neuromuscular Electrical Stimulation Systems, Washington DC, US |
| Decision | Substantially Equivalent, Nov 14, 2001 |
| Received | Aug 16, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012823
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.