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FDA 510(k)

EEG MODEL 24/32

K-Number: K924179 · 1993-06-22

ApplicantLama Engineering, Inc.
Decision Date1993-06-22
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EEG MODEL 24/32 is the device name listed in this FDA 510(k) record. The listed applicant is Lama Engineering, Inc.. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K924179. 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 EEG MODEL 24/32?

EEG MODEL 24/32 is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Lama Engineering, Inc.. The 510(k) number is K924179.

When did EEG MODEL 24/32 receive FDA 510(k) clearance?

EEG MODEL 24/32 received FDA 510(k) clearance on 1993-06-22, under 510(k) number K924179.

Who is the listed applicant for EEG MODEL 24/32?

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

What is the FDA product code for EEG MODEL 24/32?

The FDA product code for EEG MODEL 24/32 is GWQ.

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Related Devices (Code: GWQ)

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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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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