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FDA 510(k)

SNAP EEG MONITOR

K-Number: K020218 · 2002-04-22

ApplicantNicolet Biomedical, Inc.
Decision Date2002-04-22
Product CodeOLW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SNAP EEG MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Biomedical, Inc.. It received FDA 510(k) clearance on 2002-04-22 under 510(k) number K020218. The device is classified under product code OLW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNAP EEG MONITOR?

SNAP EEG MONITOR is a medical device that received FDA 510(k) clearance on 2002-04-22. The listed applicant is Nicolet Biomedical, Inc.. The 510(k) number is K020218.

When did SNAP EEG MONITOR receive FDA 510(k) clearance?

SNAP EEG MONITOR received FDA 510(k) clearance on 2002-04-22, under 510(k) number K020218.

Who is the listed applicant for SNAP EEG MONITOR?

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

What is the FDA product code for SNAP EEG MONITOR?

The FDA product code for SNAP EEG MONITOR is OLW.

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Other records listing Nicolet Biomedical, Inc. as applicant

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.

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Related Devices (Code: OLW)

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.

K260907BIS™ Advance pEEG ModuleCovidien LPK260880SedLine Sedation MonitorMasimo CorporationK230693BIS™ Advance Monitoring SystemCovidien, LLCK213273Brain Anesthesia Response Monitor (Bar Monitor)Cortical Dynamics , Ltd.K203113Masimo SedLine Sedation Monitor and AccessoriesMasimo CorporationK202621NeuroSENSE Monitoring System, Model NS-901Neurowave Systems, 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.

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