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FDA 510(k)

5MP MONOCHROME LCD MONITOR, RADIFORCE GX530

K-Number: K112354 · 2011-11-30

Decision Date2011-11-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

5MP MONOCHROME LCD MONITOR, RADIFORCE GX530 is the device name listed in this FDA 510(k) record. The listed applicant is Eizo Nanao Corporation. It received FDA 510(k) clearance on 2011-11-30 under 510(k) number K112354. 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 5MP MONOCHROME LCD MONITOR, RADIFORCE GX530?

5MP MONOCHROME LCD MONITOR, RADIFORCE GX530 is a medical device that received FDA 510(k) clearance on 2011-11-30. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K112354.

When did 5MP MONOCHROME LCD MONITOR, RADIFORCE GX530 receive FDA 510(k) clearance?

5MP MONOCHROME LCD MONITOR, RADIFORCE GX530 received FDA 510(k) clearance on 2011-11-30, under 510(k) number K112354.

Who is the listed applicant for 5MP MONOCHROME LCD MONITOR, RADIFORCE GX530?

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

What is the FDA product code for 5MP MONOCHROME LCD MONITOR, RADIFORCE GX530?

The FDA product code for 5MP MONOCHROME LCD MONITOR, RADIFORCE GX530 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.

Other records listing Eizo Nanao Corporation 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.

View all 34 devices →

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.

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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