510(k) K220530 ยท KOI Stimulator, Nerve, Peripheral, Electric
Tetragraph Neuromuscular Transmission Monitor
| Applicant | Senzime AB, Uppsala, SE |
| Decision | Substantially Equivalent, Aug 17, 2022 |
| Received | Feb 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220530
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.