510(k) K250033
K250033 is an FDA 510(k) premarket notification submitted by Guangzhou Pinzhi Medical Technology Co., Ltd. for the device "Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E)". The FDA issued a decision of Substantially Equivalent on April 7, 2025. The device falls under product code NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter), a Class II device regulated under 21 CFR 882.5890.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 7, 2025
- Date Received
- January 7, 2025
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Nerve, Transcutaneous, Over-The-Counter
- Device Class
- Class II
- Regulation Number
- 882.5890
- Review Panel
- NE
- Submission Type
TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES