510(k) K213316 ยท KOI Stimulator, Nerve, Peripheral, Electric
Life Scope PT BSM-1700 Series, AY Series, Data Acquisition Unit, LIFE SCOPE BSM 6000 SERIES BEDSIDE MONITORING SYSTEM, Nihon Kohden CSM-1901 BEDSIDE MONITORING SYSTEM
| Applicant | Nihon Kohden Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Dec 29, 2021 |
| Received | Oct 4, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213316
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.