Breg Vpulse W/O Pads
by Breg, Inc.
Breg Vpulse W/O Pads (C00001) is a Class II device made by Breg, Inc., cleared under FDA 510(k) K122640 on 22 Feb 2013 and listed in FDA GUDID since 15 Aug 2016 (UDI-DI 00672736064818), 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 | Number00672736064818 | Date15 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK122640 | Date22 Feb 2013 | StatusActive |
Official records
- AccessGUDID record 00672736064818
- FDA 510(k) database K122640
Across registries
- FDA 510(k) K122640 decided 22 Feb 2013 Active
- FDA GUDID UDI-DI 00672736064818 listed 15 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K122640
- Listed FDA GUDID 00672736064818
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Breg
- Generic name
- Sequential venous compression system inflator
- Model / Ref / Catalog
- VPULSE W/O PADS, C00001
- Primary DI / UDI-DI
- 00672736064818
- 510(k) Number
- FDA product code
- JOW
- GMDN term
- Sequential venous compression system inflator
- Device class
- Class II
- Regulation number
- 870.5800
- GUDID distribution status
- In Commercial Distribution
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