510(k) K011308 ยท BXN Stimulator, Nerve, Battery-Powered
MULTISTIM
| Applicant | Pajunk GmbH, Flemington NJ, US |
| Decision | Substantially Equivalent, Nov 29, 2001 |
| Received | Apr 30, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011308
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.