# K062482: Vented Vial Adapter Transfer Device

- Pathway: 510(k) (Traditional)
- Applicant: Medimop Medical Projects, Ltd.
- Decided: Nov 3, 2006 after 71 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: 2 generations back to K925401 (1993). 6 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K963583: Mixject Dispensing Pin/with Detachable Vial Holder/with Detachable Vial Holder and Preattached Needle, Medimop Medical Projects, Ltd. (1996) Summary page 1.
- K001293: Modification to Mixject Dispensing Pin/with Detachable Vial Holder/with Detachable Vial Holder and Pre-Attached Needle, Medimop Medical Projects, Ltd. (2000) Summary page 1.
- K031861: MIX2VIAL Transfer Device, Medimop Medical Projects, Ltd. (2003) Summary page 1.
- K983794: Chemo Mini Spike Plus, B. Braun of America, Inc. (1999) Summary page 1.
- K974198: Taky-Spike Plus, Clinico (1997) Summary page 1.

## Most influential descendants
- K160503: Vented Vial Adapter Transfer Device - 13mm (2016), 2 descendants of its own
- K221406: Vented Vial Transfer Pin (2022), 0 descendants of its own
- K213513: Vented Vial Adapter 20mm (2022), 0 descendants of its own
- K122265: Vialok Single Vial Access Device Vented (2012), 0 descendants of its own

## Indications for use
Transfer and Mixing of drugs contained in vials

Source page: https://510kreport.com/device/K062482
Methodology: https://510kreport.com/methodology