510(k) K955031 ยท KOI Stimulator, Nerve, Peripheral, Electric
MAXISTIM
| Applicant | Life-Tech Intl., Inc., Houston TX, US |
| Decision | Substantially Equivalent, Dec 10, 1996 |
| Received | Nov 2, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955031
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.