# K042410: Baxject II

- Pathway: 510(k) (Abbreviated)
- Applicant: Baxter Healthcare Corp
- Decided: Oct 8, 2004 after 31 days
- Product code: LHI (Set, I.V. Fluid Transfer)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K001831 (2000). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001831: Needleless Transfer Device, Medimop Medical Projects, Ltd. (2000) Summary page 1.

## Most influential descendants
- K092318: Baxject II HI-Flow Needleless Transfer Device (2009), 0 descendants of its own

## Indications for use
The BAXJECT II Needleless Transfer Device is intended for transferring and mixing drugs contained in two vials into a syringe.

Source page: https://510kreport.com/device/K042410
Methodology: https://510kreport.com/methodology