# K221406: Vented Vial Transfer Pin

- Pathway: 510(k) (Traditional)
- Applicant: Jiangsu Caina Medical Co.,Ltd
- Decided: Oct 28, 2022 after 165 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: 4 generations back to K925401 (1993). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160503: Vented Vial Adapter Transfer Device - 13mm, Medimop Medical Projects, Ltd. (2016) Summary page 5.

## Indications for use
The Vented Vial Transfer Pin is intended for the transfer and mixing of drugs contained in a vial.

Source page: https://510kreport.com/device/K221406
Methodology: https://510kreport.com/methodology