510(k) K092292 ยท ETN Stimulator, Nerve
CHECKPOINT
| Applicant | Ndi Medical, LLC, Cleveland OH, US |
| Decision | Substantially Equivalent, Oct 28, 2009 |
| Received | Jul 29, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092292
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.