IV Plus N0669

by Nexus Medical, LLC

IV Plus N0669 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 8 Sep 2022 (UDI-DI 10815879021547), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10815879021547 UDI-DI	Date8 Sep 2022Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK080976	Date10 Nov 2008Decided	StatusActive

Official records

AccessGUDID record UDI-DI 10815879021547
FDA 510(k) database 510(k) number K080976

Across registries

2 registries list this device

FDA 510(k) K080976 decided 10 Nov 2008 Active
FDA GUDID UDI-DI 10815879021547 listed 8 Sep 2022 Listed

Timeline

2 dated events

10 Nov 2008 Cleared FDA 510(k) K080976
8 Sep 2022 Listed FDA GUDID 10815879021547

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: IV Plus
Generic name: Fluid transfer set, general-purpose
Model / reference: N0669

Primary DI / UDI-DI: 10815879021547
510(k) Number: K080976
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.

Other devices from Nexus Medical, LLC

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Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)