# K160503: Vented Vial Adapter Transfer Device - 13mm

- Pathway: 510(k) (Special)
- Applicant: Medimop Medical Projects, Ltd.
- Decided: May 4, 2016 after 70 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: 3 generations back to K925401 (1993). 7 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062482: Vented Vial Adapter Transfer Device, Medimop Medical Projects, Ltd. (2006) Summary page 4.

## Most influential descendants
- K221406: Vented Vial Transfer Pin (2022), 0 descendants of its own
- K213513: Vented Vial Adapter 20mm (2022), 0 descendants of its own

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

Source page: https://510kreport.com/device/K160503
Methodology: https://510kreport.com/methodology