510(k) K220976 ยท KOI Stimulator, Nerve, Peripheral, Electric
Life Scope PT BSM-1700 Series Bedside Monitor
| Applicant | Nihon Kohden Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Jul 21, 2022 |
| Received | Apr 4, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K220976
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.