# K010703: Inter-Vial

- Pathway: 510(k) (Traditional)
- Applicant: Duoject Medical Systems, Inc.
- Decided: Jun 25, 2001 after 108 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; 1 cites 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K041691: Clip 'N'ject Reconstitution System (Clip 'N'ject (2004), 3 descendants of its own
- K070584: Smart-Rod (2008), 2 descendants of its own
- K133097: E-Z Link (2014), 1 descendant of its own
- K161800: OnSite-IV (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K010703
Methodology: https://510kreport.com/methodology