K250033
- 510(k) number
- K250033
- Device name
- Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E)
- Applicant
- Guangzhou Pinzhi Medical Technology Co., Ltd. CN
- Product code
- NUH — Stimulator, Nerve, Transcutaneous, Over-The-Counter
- Decision date
- 2025-04-07
- Date received
- 2025-01-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K250033
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.