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FDA 510(k)

RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS

K-Number: K070131 · 2007-02-15

ApplicantEizo Nanao Corporation
Decision Date2007-02-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS 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 2007-02-15 under 510(k) number K070131. 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 RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS?

RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS is a medical device that received FDA 510(k) clearance on 2007-02-15. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K070131.

When did RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS receive FDA 510(k) clearance?

RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS received FDA 510(k) clearance on 2007-02-15, under 510(k) number K070131.

Who is the listed applicant for RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS?

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 RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS?

The FDA product code for RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS is LLZ.

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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)

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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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