510(k) K080219 ยท GZI Stimulator, Neuromuscular, External Functional
MODIFICATION TO:NESS L300
| Applicant | Ness-Neuromuscular Electrical Stimulation Systems, Valencia CA, US |
| Decision | Substantially Equivalent, Feb 28, 2008 |
| Received | Jan 29, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080219
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.