510(k) K061172 ยท BXN Stimulator, Nerve, Battery-Powered
PAJUNK MULTISTIM SENSOR NERVE STIMULATORS
| Applicant | PAJUNK GmbH Medizintechnologie, Mount Dora FL, US |
| Decision | Substantially Equivalent, Oct 17, 2006 |
| Received | Apr 27, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061172
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.