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FDA 510(k)

AMPLIFIER MODEL N3B-EEG

K-Number: K771683 · 1977-09-20

ApplicantHoneywell, Inc.
Decision Date1977-09-20
Product CodeGWL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AMPLIFIER MODEL N3B-EEG is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1977-09-20 under 510(k) number K771683. The device is classified under product code GWL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMPLIFIER MODEL N3B-EEG?

AMPLIFIER MODEL N3B-EEG is a medical device that received FDA 510(k) clearance on 1977-09-20. The listed applicant is Honeywell, Inc.. The 510(k) number is K771683.

When did AMPLIFIER MODEL N3B-EEG receive FDA 510(k) clearance?

AMPLIFIER MODEL N3B-EEG received FDA 510(k) clearance on 1977-09-20, under 510(k) number K771683.

Who is the listed applicant for AMPLIFIER MODEL N3B-EEG?

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

What is the FDA product code for AMPLIFIER MODEL N3B-EEG?

The FDA product code for AMPLIFIER MODEL N3B-EEG is GWL.

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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.

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