510(k) K250033 ยท NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E)
| Applicant | Guangzhou Pinzhi Medical Technology Co., Ltd., Guangzhou, CN |
| Decision | Substantially Equivalent, Apr 7, 2025 |
| Received | Jan 7, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250033
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.