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FDA 510(k)

RADIFORCE RX240

K-Number: K113844 · 2012-02-27

ApplicantEizo Nanao Corporation
Decision Date2012-02-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIFORCE RX240 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 2012-02-27 under 510(k) number K113844. 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 RX240?

RADIFORCE RX240 is a medical device that received FDA 510(k) clearance on 2012-02-27. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K113844.

When did RADIFORCE RX240 receive FDA 510(k) clearance?

RADIFORCE RX240 received FDA 510(k) clearance on 2012-02-27, under 510(k) number K113844.

Who is the listed applicant for RADIFORCE RX240?

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 RX240?

The FDA product code for RADIFORCE RX240 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)

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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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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