Upper Arm Electronic Blood Pressure Monitor (U87Y series (models including U80Y, U81Y, U82Y,U83Y,U86Y U80N, U81NH), U86E series (including U82E, U80E, U80EH, U81E, U83E, U85E, U80L, U87E ), U81X series (including U81X, U80X, U82X, U83X, U81D, U82D, U83D, U81RH, U82RH) and U83Z series (including U83Z, U80Z, U81Z, U82Z, U85Z, U86Z and U87Z))
K243115 is the FDA 510(k) clearance record for Upper Arm Electronic Blood Pressure Monitor (U87Y series (models including U80Y, U81Y, U82Y,U83Y,U86Y U80N, U81NH), U86E series (including U82E, U80E, U80EH, U81E, U83E, U85E, U80L, U87E ), U81X series (including U81X, U80X, U82X, U83X, U81D, U82D, U83D, U81RH, U82RH) and U83Z series (including U83Z, U80Z, U81Z, U82Z, U85Z, U86Z and U87Z)), a class II device, cleared for Shenzhen Urion Technology Co., Ltd. on under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive). FDA records list 8 510(k) clearances for Shenzhen Urion Technology Co., Ltd., from to . As of , FDA records show no recalls naming K243115.
Clearance record
- Decision date
- Received
- (144 days to decision)
- Product code
- DXN System, Measurement, Blood-Pressure, Non-Invasive
- Regulation
- 21 CFR 870.1130
- Device class
- Class II
- Review panel
- Cardiovascular
- Applicant
- Shenzhen Urion Technology Co., Ltd. Floor 4-6th Of Bldg. D, Jiale Science & Technology Indust, Shenzhen, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code DXN
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 2 |
| February 2026 | 4 |
| March 2026 | 2 |
| April 2026 | 5 |
| May 2026 | 3 |
| June 2026 | 4 |
| July 2026 | 2 |
| August 2026 | 4 |
| September 2026 | 2 |
| October 2026 | 0 |
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