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FDA 510(k)

MEDELEC 2110 AND 2114 EEG

K-Number: K922548 · 1992-11-03

ApplicantMedelec Intl. Corp.
Decision Date1992-11-03
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDELEC 2110 AND 2114 EEG is the device name listed in this FDA 510(k) record. The listed applicant is Medelec Intl. Corp.. It received FDA 510(k) clearance on 1992-11-03 under 510(k) number K922548. 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 MEDELEC 2110 AND 2114 EEG?

MEDELEC 2110 AND 2114 EEG is a medical device that received FDA 510(k) clearance on 1992-11-03. The listed applicant is Medelec Intl. Corp.. The 510(k) number is K922548.

When did MEDELEC 2110 AND 2114 EEG receive FDA 510(k) clearance?

MEDELEC 2110 AND 2114 EEG received FDA 510(k) clearance on 1992-11-03, under 510(k) number K922548.

Who is the listed applicant for MEDELEC 2110 AND 2114 EEG?

The FDA 510(k) record lists Medelec Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDELEC 2110 AND 2114 EEG?

The FDA product code for MEDELEC 2110 AND 2114 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.

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