510(k) K251307
K251307 is an FDA 510(k) premarket notification submitted by Shenzhen Hingmed Medical Instrument Co., Ltd. for the device "Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i)". The FDA issued a decision of Substantially Equivalent on January 12, 2026. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Shenzhen Hingmed Medical Instrument Co., Ltd. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 12, 2026
- Date Received
- April 28, 2025
- 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