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FDA 510(k)

DEI MODEL 20 EEG

K-Number: K961718 · 1996-08-27

ApplicantDiscovery Engineering Intl., Inc.
Decision Date1996-08-27
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DEI MODEL 20 EEG is the device name listed in this FDA 510(k) record. The listed applicant is Discovery Engineering Intl., Inc.. It received FDA 510(k) clearance on 1996-08-27 under 510(k) number K961718. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEI MODEL 20 EEG?

DEI MODEL 20 EEG is a medical device that received FDA 510(k) clearance on 1996-08-27. The listed applicant is Discovery Engineering Intl., Inc.. The 510(k) number is K961718.

When did DEI MODEL 20 EEG receive FDA 510(k) clearance?

DEI MODEL 20 EEG received FDA 510(k) clearance on 1996-08-27, under 510(k) number K961718.

Who is the listed applicant for DEI MODEL 20 EEG?

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

What is the FDA product code for DEI MODEL 20 EEG?

The FDA product code for DEI MODEL 20 EEG is HCC.

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Related Devices (Code: HCC)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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