UltraCheck BP Cuffs
by Statcorp Medical 169 variants
UltraCheck BP Cuffs (US2635FL) is a Class II device made by Statcorp Medical, cleared under FDA 510(k) K954282 on 6 Feb 1996 and listed in FDA GUDID since 19 Oct 2016 (UDI-DI 10841522110504), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10841522110504 | Date19 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK954282 | Date6 Feb 1996 | StatusActive |
Official records
- AccessGUDID record 10841522110504
- FDA 510(k) database K954282
Across registries
- FDA 510(k) K954282 decided 6 Feb 1996 Active
- FDA GUDID UDI-DI 10841522110504 listed 19 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K954282
- Listed FDA GUDID 10841522110504
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ultracheck
- Generic name
- Blood pressure cuff, reusable
- Model / Ref / Catalog
- UltraCheck BP Cuffs, US2635FL
- Primary DI / UDI-DI
- 10841522110504
- 510(k) Number
- FDA product code
- DXQ
- GMDN term
- Blood pressure cuff, reusable
- Device class
- Class II
- Regulation number
- 870.1120
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code DXQ (blood pressure cuff).
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- ULTRACUFF BLOOD PRESSURE CUFF AND INFLATION BAG by Statcorp, Inc.
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- CUFFABLE by Biomedical Dynamics, Inc.
- MDF® MDF840D04 by MDF Instruments Medifriend Inc.
- Aneroid Sphygmomanometer by Wuxi Exanovo Medical Instrument Co., Ltd.