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FDA 510(k)

20.1 MONOCHROME LCD MONITOR, RADIFORCE G21

K-Number: K024358 · 2003-03-25

ApplicantEizo Nanao Corporation
Decision Date2003-03-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

20.1 MONOCHROME LCD MONITOR, RADIFORCE G21 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 2003-03-25 under 510(k) number K024358. 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 20.1 MONOCHROME LCD MONITOR, RADIFORCE G21?

20.1 MONOCHROME LCD MONITOR, RADIFORCE G21 is a medical device that received FDA 510(k) clearance on 2003-03-25. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K024358.

When did 20.1 MONOCHROME LCD MONITOR, RADIFORCE G21 receive FDA 510(k) clearance?

20.1 MONOCHROME LCD MONITOR, RADIFORCE G21 received FDA 510(k) clearance on 2003-03-25, under 510(k) number K024358.

Who is the listed applicant for 20.1 MONOCHROME LCD MONITOR, RADIFORCE G21?

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 20.1 MONOCHROME LCD MONITOR, RADIFORCE G21?

The FDA product code for 20.1 MONOCHROME LCD MONITOR, RADIFORCE G21 is LLZ.

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Other records listing Eizo Nanao Corporation as applicant

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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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