510(k) K120853 ยท GZI Stimulator, Neuromuscular, External Functional
NESS L300 SYSTEM KIT, LEFT, NESS L300 SYSTEM KIT, RIGHT, SMALL NESS L300 SYSTEM KIT, RIGHT, SMALL NESS L300 SYSTEM KIT,
| Applicant | Bioness, Inc., Valencia CA, US |
| Decision | Substantially Equivalent, Apr 20, 2012 |
| Received | Mar 21, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120853
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.