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FDA 510(k)

LCD MONITOR, RADIFORCE G11, G31, G51

K-Number: K032026 · 2003-08-27

Decision Date2003-08-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LCD MONITOR, RADIFORCE G11, G31, G51 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 2003-08-27 under 510(k) number K032026. 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 LCD MONITOR, RADIFORCE G11, G31, G51?

LCD MONITOR, RADIFORCE G11, G31, G51 is a medical device that received FDA 510(k) clearance on 2003-08-27. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K032026.

When did LCD MONITOR, RADIFORCE G11, G31, G51 receive FDA 510(k) clearance?

LCD MONITOR, RADIFORCE G11, G31, G51 received FDA 510(k) clearance on 2003-08-27, under 510(k) number K032026.

Who is the listed applicant for LCD MONITOR, RADIFORCE G11, G31, G51?

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 LCD MONITOR, RADIFORCE G11, G31, G51?

The FDA product code for LCD MONITOR, RADIFORCE G11, G31, G51 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.

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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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