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FDA 510(k)

MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL

K-Number: K090215 · 2009-04-15

ApplicantNec Display Solutions , Ltd.
Decision Date2009-04-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL is the device name listed in this FDA 510(k) record. The listed applicant is Nec Display Solutions , Ltd.. It received FDA 510(k) clearance on 2009-04-15 under 510(k) number K090215. 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 MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL?

MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL is a medical device that received FDA 510(k) clearance on 2009-04-15. The listed applicant is Nec Display Solutions , Ltd.. The 510(k) number is K090215.

When did MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL receive FDA 510(k) clearance?

MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL received FDA 510(k) clearance on 2009-04-15, under 510(k) number K090215.

Who is the listed applicant for MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL?

The FDA 510(k) record lists Nec Display Solutions , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL?

The FDA product code for MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL is LLZ.

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Other records listing Nec Display Solutions , Ltd. 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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