# K261273: Neurophet AQUA

- Pathway: 510(k) (Special)
- Applicant: Neurophet., Inc.
- Decided: May 15, 2026 after 28 days
- Product code: QIH (Automated Radiological Image Processing Software)
- Device class: 2
- Regulation: 21 CFR 892.2050
- 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 K061855 (2006). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K242215: Neurophet AQUA (V3.1), Neurophet., Inc. (2024) Summary page 6.

## Indications for use
Neurophet AQUA is intended for Automatic labeling, visualization and volumetric quantification of segmentable brain structures and lesions from a set of MR images. Volumetric data may be compared to reference percentile data.

Source page: https://510kreport.com/device/K261273
Methodology: https://510kreport.com/methodology