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FDA 510(k)

MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK

K-Number: K083332 · 2009-01-09

Decision Date2009-01-09
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK 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 2009-01-09 under 510(k) number K083332. 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 MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK?

MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK is a medical device that received FDA 510(k) clearance on 2009-01-09. The listed applicant is Nec Display Solutions , Ltd.. The 510(k) number is K083332.

When did MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK receive FDA 510(k) clearance?

MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK received FDA 510(k) clearance on 2009-01-09, under 510(k) number K083332.

Who is the listed applicant for MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK?

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 MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK?

The FDA product code for MD21M 21.3 DIAGNOSTIC IMAGING LCD MONITOR, MODEL L218TK 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 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.

View all 12 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

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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