510(k) K260670
K260670 is an FDA 510(k) premarket notification submitted by Jiangsu Yuyue Medical Equipment & Supply Co., Ltd. for the device "YUWELL® Electronic Blood Pressure Monitor". The FDA issued a decision of Substantially Equivalent on Oct 28, 2026. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Jiangsu Yuyue Medical Equipment & Supply Co., Ltd. has 15 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 28, 2026
- Date Received
- Mar 2, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- System, Measurement, Blood-Pressure, Non-Invasive
- Device Class
- Class II
- Regulation Number
- 870.1130
- Review Panel
- CV
- Submission Type
- 510(k)