IV Plus AD1002
IV Plus AD1002 is a fluid transfer set (FDA Class II; FDA product code LHI, Set, I.V. Fluid Transfer) made by Nexus Medical, LLC, cleared under FDA 510(k) K080976 on 10 Nov 2008 and listed in FDA GUDID since 16 Sep 2024 (UDI-DI 10815879021745), 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 | Number10815879021745 | Date16 Sep 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK080976 | Date10 Nov 2008 | StatusActive |
Official records
- AccessGUDID record 10815879021745
- FDA 510(k) database K080976
Across registries
- FDA 510(k) K080976 decided 10 Nov 2008 Active
- FDA GUDID UDI-DI 10815879021745 listed 16 Sep 2024 Listed
Timeline
- Cleared FDA 510(k) K080976
- Listed FDA GUDID 10815879021745
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- IV Plus
- Generic name
- Fluid transfer set, general-purpose
- Model / reference
- AD1002
- Primary DI / UDI-DI
- 10815879021745
- 510(k) Number
- FDA product code
- LHI
- GMDN term
- Fluid transfer set, general-purpose
- Device class
- Class II
- Regulation number
- 880.5440
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Fluid transfer set, general-purpose.