510(k) K122784 ยท GZI Stimulator, Neuromuscular, External Functional
NESS L300 SYSTEM KIT, LEF MODEL LG3-5100; NESS L300 SYSTEM KIT, RIGHT MODEL LG3-5000; SMALL NESS L300 SYSTEM KIT, RIGHT
| Applicant | Bioness, Inc., Valencia CA, US |
| Decision | Substantially Equivalent, Dec 27, 2012 |
| Received | Sep 11, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122784
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.