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

FDA 510(k)

NEUROAMP EEG AMPLIFIER

K-Number: K974495 · 1998-02-26

ApplicantNeurocorp, Ltd.
Decision Date1998-02-26
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROAMP EEG AMPLIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Neurocorp, Ltd.. It received FDA 510(k) clearance on 1998-02-26 under 510(k) number K974495. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROAMP EEG AMPLIFIER?

NEUROAMP EEG AMPLIFIER is a medical device that received FDA 510(k) clearance on 1998-02-26. The listed applicant is Neurocorp, Ltd.. The 510(k) number is K974495.

When did NEUROAMP EEG AMPLIFIER receive FDA 510(k) clearance?

NEUROAMP EEG AMPLIFIER received FDA 510(k) clearance on 1998-02-26, under 510(k) number K974495.

Who is the listed applicant for NEUROAMP EEG AMPLIFIER?

The FDA 510(k) record lists Neurocorp, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEUROAMP EEG AMPLIFIER?

The FDA product code for NEUROAMP EEG AMPLIFIER is GWQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: GWQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261604Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)Neuroelectrics Barcelona S.L.U.K260455New Wave SystemZeto, Inc.K233403Flexset SystemZeto, Inc.K231366Neuronaute PlusBioserenity SasK221959Q21Neurofield, Inc.K231457SPARK ScanSpark Neuro, 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.

↑