Neurophet AQUA AD Plus
K-Number: K252496 · 2026-01-29
ApplicantNeurophet., Inc.
Decision Date2026-01-29
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Neurophet AQUA AD Plus is a medical device manufactured by Neurophet., Inc.. It received FDA 510(k) clearance on 2026-01-29 under approval number K252496. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Neurophet AQUA AD Plus?
Neurophet AQUA AD Plus is a medical device that received FDA 510(k) clearance on 2026-01-29. It is manufactured by Neurophet., Inc.. The 510(k) number is K252496.
When was Neurophet AQUA AD Plus approved by the FDA?
Neurophet AQUA AD Plus received FDA 510(k) clearance on 2026-01-29, under approval number K252496.
What company makes Neurophet AQUA AD Plus?
Neurophet AQUA AD Plus is manufactured by Neurophet., Inc..
What is the FDA product code for Neurophet AQUA AD Plus?
The FDA product code for Neurophet AQUA AD Plus is QIH.
Other Devices by Neurophet., Inc.
Related Devices (Code: QIH)
K191647QLAB Advanced Quantification SoftwarePhilips Health Care
K191171EchoGo CoreUltromics, Ltd.
K201195syngo.via MI Workflows, syngo MBFSiemens Medical Solutions USA, Inc.
K202013WRDensity by Whiterabbit.aiWhiterabbit.Ai, Inc.
K202546LVivo SeamlessDia Imaging Analysis, Ltd.
K193283AI-Rad Companion Prostate MRSiemens Medical Solutions USA, Inc.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.