Accu-Read BP00-3101
Accu-Read BP00-3101 is a Class II device made by Reprocessing Products Corp, cleared under FDA 510(k) K171889 on 19 Dec 2017 and listed in FDA GUDID since 30 Aug 2019 (UDI-DI 00858293006441), active as of 22 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 | Number00858293006441 | Date30 Aug 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK171889 | Date19 Dec 2017 | StatusActive |
Official records
- AccessGUDID record 00858293006441
- FDA 510(k) database K171889
Across registries
- FDA 510(k) K171889 decided 19 Dec 2017 Active
- FDA GUDID UDI-DI 00858293006441 listed 30 Aug 2019 Listed
Timeline
- Cleared FDA 510(k) K171889
- Listed FDA GUDID 00858293006441
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Accu-Read
- Generic name
- Blood pressure cuff, reusable
- Model / reference
- BP00-3101
- Description
- BP Cuff, Adult Thigh, 1 Tube BP00-3105 = 5 pack
- Primary DI / UDI-DI
- 00858293006441
- 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 in this category
Other devices filed under Blood pressure cuff, reusable.