510(k) K162407 ยท GZI Stimulator, Neuromuscular, External Functional
L300 Go System
| Applicant | Bioness, Inc., Valencia CA, US |
| Decision | Substantially Equivalent, Jan 27, 2017 |
| Received | Aug 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162407
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.