Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HippoMind (v1.0)

K-Number: K251881 · 2025-12-03

ApplicantHippoclinic
Decision Date2025-12-03
Product CodeOLT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HippoMind (v1.0) is a medical device manufactured by Hippoclinic. It received FDA 510(k) clearance on 2025-12-03 under approval number K251881. The device is classified under product code OLT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HippoMind (v1.0)?

HippoMind (v1.0) is a medical device that received FDA 510(k) clearance on 2025-12-03. It is manufactured by Hippoclinic. The 510(k) number is K251881.

When was HippoMind (v1.0) approved by the FDA?

HippoMind (v1.0) received FDA 510(k) clearance on 2025-12-03, under approval number K251881.

What company makes HippoMind (v1.0)?

HippoMind (v1.0) is manufactured by Hippoclinic.

What is the FDA product code for HippoMind (v1.0)?

The FDA product code for HippoMind (v1.0) is OLT.

Related Devices (Code: OLT)

K192572CNS EnvisionMoberg Research, Inc. K190760Cadwell Bolt SoftwareCadwell Industries, Inc. K191322E-EEGX, N-EEGXGE Healthcare Finland Oy K220254Neuron-Spectrum-AM with Neuron-Spectrum.NET SoftwareNeurosoft , Ltd. K213299Wireless EEG SystemPascall Systems, Inc. K240593VEEGix EEG SystemNeuroServo, 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.

↑