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FDA 510(k)

MONOCHROME LCD MONITOR, MODEL RADIFORCE G22

K-Number: K041597 · 2004-06-24

Decision Date2004-06-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MONOCHROME LCD MONITOR, MODEL RADIFORCE G22 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 2004-06-24 under 510(k) number K041597. 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 MONOCHROME LCD MONITOR, MODEL RADIFORCE G22?

MONOCHROME LCD MONITOR, MODEL RADIFORCE G22 is a medical device that received FDA 510(k) clearance on 2004-06-24. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K041597.

When did MONOCHROME LCD MONITOR, MODEL RADIFORCE G22 receive FDA 510(k) clearance?

MONOCHROME LCD MONITOR, MODEL RADIFORCE G22 received FDA 510(k) clearance on 2004-06-24, under 510(k) number K041597.

Who is the listed applicant for MONOCHROME LCD MONITOR, MODEL RADIFORCE G22?

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 MONOCHROME LCD MONITOR, MODEL RADIFORCE G22?

The FDA product code for MONOCHROME LCD MONITOR, MODEL RADIFORCE G22 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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