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FDA 510(k)

10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030)

K-Number: K103724 · 2011-06-08

ApplicantEizo GmbH
Decision Date2011-06-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030) is the device name listed in this FDA 510(k) record. The listed applicant is Eizo GmbH. It received FDA 510(k) clearance on 2011-06-08 under 510(k) number K103724. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030)?

10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030) is a medical device that received FDA 510(k) clearance on 2011-06-08. The listed applicant is Eizo GmbH. The 510(k) number is K103724.

When did 10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030) receive FDA 510(k) clearance?

10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030) received FDA 510(k) clearance on 2011-06-08, under 510(k) number K103724.

Who is the listed applicant for 10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030)?

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

What is the FDA product code for 10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030)?

The FDA product code for 10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030) is LLZ.

Related Clinical Trials

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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Other records listing Eizo GmbH as applicant

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.

K112645RADIFORCE LARGE MONITOR SYSTEMK0813575MP GRAYSCALE FLAT PANEL DISPLAY, MODEL, 6GF6201-5C$2# (WHERE $ = A-Z AND # = 0-9)

Related Devices (Code: LLZ)

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

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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