# K001831: Needleless Transfer Device

- Pathway: 510(k) (Traditional)
- Applicant: Medimop Medical Projects, Ltd.
- Decided: Jul 11, 2000 after 25 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
No predicates in its family tree.
4 later devices descend from it; 3 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K042410: Baxject II (2004), 1 descendant of its own
- K020666: Duploject Easy-Prep System 1ML, 2ML, 5ML (2002), 1 descendant of its own
- K092318: Baxject II HI-Flow Needleless Transfer Device (2009), 0 descendants of its own
- K071126: Cryoseal FS Applicator System (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K001831
Methodology: https://510kreport.com/methodology