FDA 510(k)

ELECTROENCEPHALOGRAPH EEG

K-Number: K850259 · 1985-04-11

Decision Date1985-04-11

Product CodeGWQ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

ELECTROENCEPHALOGRAPH EEG is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Biomedical Instruments. It received FDA 510(k) clearance on 1985-04-11 under 510(k) number K850259. 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 ELECTROENCEPHALOGRAPH EEG?

ELECTROENCEPHALOGRAPH EEG is a medical device that received FDA 510(k) clearance on 1985-04-11. The listed applicant is Nicolet Biomedical Instruments. The 510(k) number is K850259.

When did ELECTROENCEPHALOGRAPH EEG receive FDA 510(k) clearance?

ELECTROENCEPHALOGRAPH EEG received FDA 510(k) clearance on 1985-04-11, under 510(k) number K850259.

Who is the listed applicant for ELECTROENCEPHALOGRAPH EEG?

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

What is the FDA product code for ELECTROENCEPHALOGRAPH EEG?

The FDA product code for ELECTROENCEPHALOGRAPH EEG is GWQ.

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Related Devices (Code: GWQ)

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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.