# K240748: nextaro® v, 20/20

- Pathway: 510(k) (Special)
- Applicant: Sfm Medical Devices GmbH
- Decided: Apr 16, 2024 after 28 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 K031861 (2003). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183187: nextaro Transfer System, nextaro va, Sfm Medical Devices GmbH (2019) Summary page 5.

## Indications for use
The nextaro® v, 20/20 is indicated for the transfer and mixing of drugs contained in vials.

Source page: https://510kreport.com/device/K240748
Methodology: https://510kreport.com/methodology