Vasocuff Cuff-210
Vasocuff Cuff-210 is a Class II device made by Newman Medical, cleared under FDA 510(k) K152468 on 29 Oct 2015 and listed in FDA GUDID since 6 Jul 2021 (UDI-DI 00852785008685), 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 | Number00852785008685 | Date6 Jul 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK152468 | Date29 Oct 2015 | StatusActive |
Official records
- AccessGUDID record 00852785008685
- FDA 510(k) database K152468
Across registries
- FDA 510(k) K152468 decided 29 Oct 2015 Active
- FDA GUDID UDI-DI 00852785008685 listed 6 Jul 2021 Listed
Timeline
- Cleared FDA 510(k) K152468
- Listed FDA GUDID 00852785008685
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vasocuff
- Generic name
- Blood pressure cuff, reusable
- Model / Ref / Catalog
- CUFF-210
- Primary DI / UDI-DI
- 00852785008685
- 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.