FDA 510(k) Applications Submitted by Guangzhou Pinzhi Medical Technology Co., LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K250033 | 01/07/2025 | Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E) | Guangzhou Pinzhi Medical Technology Co., LTD |
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