Arm Blood Pressure Monitor Models: ARM-30C+; ARM-30M+; ARM-HA101+; ARM-3060; XS Pro; ARM-30G1; ARM-30H; Visomat double comfort; Visomat comfort 20/40 BT; ARM-3080; ARM-3081; ARM-3082; ARM-3103; ARM-3200; ARM-115; ARM-111; ARM-3102; ARM-3100; ARM-3101; SBM 15; ARM-30W; ARM-30J; ARM-30F-XL; ARM-3024-XL; ARM-3025-XL; ARM-3062-XL; 9S Pro
K260276 is the FDA 510(k) clearance record for Arm Blood Pressure Monitor Models: ARM-30C+; ARM-30M+; ARM-HA101+; ARM-3060; XS Pro; ARM-30G1; ARM-30H; Visomat double comfort; Visomat comfort 20/40 BT; ARM-3080; ARM-3081; ARM-3082; ARM-3103; ARM-3200; ARM-115; ARM-111; ARM-3102; ARM-3100; ARM-3101; SBM 15; ARM-30W; ARM-30J; ARM-30F-XL; ARM-3024-XL; ARM-3025-XL; ARM-3062-XL; 9S Pro, a class II device, cleared for Shenzhen AOJ Medical Technology Co., Ltd. on under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive). FDA records list 17 510(k) clearances for Shenzhen AOJ Medical Technology Co., Ltd., from to . As of , FDA records show no recalls naming K260276.
Clearance record
- Decision date
- Received
- (62 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 AOJ Medical Technology Co., Ltd. Rm. 301&4-5f, Block A, Bldg. A, Jingfa Intelligent, Shenzhen, CN
- 510(k) summary
- Statement
- 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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