# K183187: nextaro Transfer System, nextaro va

- Pathway: 510(k) (Traditional)
- Applicant: Sfm Medical Devices GmbH
- Decided: Mar 15, 2019 after 116 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: 1 generation back to K031861 (2003). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031861: MIX2VIAL Transfer Device, Medimop Medical Projects, Ltd. (2003) Summary page 4.

## Most influential descendants
- K241976: nextaro® va, 15mm, 5µm (2024), 0 descendants of its own
- K240748: nextaro® v, 20/20 (2024), 0 descendants of its own

## Indications for use
The nextaro® Transfer System and nextaro® va is indicated for the transfer and mixing of drugs contained in vials.

Source page: https://510kreport.com/device/K183187
Methodology: https://510kreport.com/methodology