510(k) K103343 ยท GZI Stimulator, Neuromuscular, External Functional
L300 PLUS SYSTEM (RIGHT, LEFT), L300 PLUS SYSTEM UPGRADE KIT (RIGHT, LEFT)
| Applicant | Bioness, Inc., Valencia CA, US |
| Decision | Substantially Equivalent, Apr 29, 2011 |
| Received | Nov 15, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103343
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.