NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)
K253089 is the FDA 510(k) clearance record for NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722), a class II device, cleared for Shenzhen Best Electronics Co., Ltd. on under FDA product code DXQ (Blood Pressure Cuff). FDA's definition for product code DXQ reads: "A blood pressure cuff is a device that has an inflatable bladder in an elastic sleeve (cuff) with a mechanism for inflating the bladder. The cuff is used to determine a subject's blood pressure". FDA records list 2 510(k) clearances for Shenzhen Best Electronics Co., Ltd., from to . As of , FDA records show no recalls naming K253089.
Clearance record
- Decision date
- Received
- (143 days to decision)
- Product code
- DXQ Blood Pressure Cuff
- Regulation
- 21 CFR 870.1120
- Device class
- Class II
- Review panel
- Cardiovascular
- Applicant
- Shenzhen Best Electronics Co., Ltd. 605 #59 Bldg., The Second Industrial Park, Shenzhen, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code DXQ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 1 |
| February 2026 | 1 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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