# K252496: Neurophet AQUA AD Plus

- Pathway: 510(k) (Traditional)
- Applicant: Neurophet., Inc.
- Decided: Jan 29, 2026 after 174 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: 9 generations back to K954874 (1996). 42 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 44 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K241098: NeuroQuant, Cortechs Labs, Inc. (2024) Summary page 6.
- K221405: Neurophet SCALE PET, Neurophet., Inc. (2022) Summary page 6.

## Most influential descendants
- K252563: Neurophet SCALE PET (2026), 0 descendants of its own

## Indications for use
Neurophet AQUA AD Plus is intended for automatic labeling, visualization, and volumetric quantification of segmentable brain structures and lesions, as well as SUVR quantification from a set of MR and PET images. Volumetric measurements may be compared to reference percentile data.

Source page: https://510kreport.com/device/K252496
Methodology: https://510kreport.com/methodology