510(k) K201949 ยท KOI Stimulator, Nerve, Peripheral, Electric
Smart Cable NMT Module and Accessories, Life Scope BSM 3000 Series and Life Scope BSM 6000 Series
| Applicant | Nihon Kohden Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, May 2, 2021 |
| Received | Jul 13, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201949
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.