Class Class II
Neurophet AQUA (V3.1) (K242215)
Description
Neurophet AQUA (V3.1) by Neurophet., Inc., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242215
Clearance Date2024-10-25
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242215
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Neurophet AQUA (V3.1) (K242215) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K220437 | Neurophet AQUA | Neurophet., Inc. | 2023 |
| K170981 | NeuroQuant | Cortechs Labs, Inc. | 2017 |
Trace the full predicate network for K242215
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.