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FDA 510(k)

21.3 INCH MONOCHROME LCD MONITOR

K-Number: K061947 · 2006-07-25

ApplicantNec Display Solutions , Ltd.
Decision Date2006-07-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

21.3 INCH MONOCHROME LCD MONITOR 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 2006-07-25 under 510(k) number K061947. 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 21.3 INCH MONOCHROME LCD MONITOR?

21.3 INCH MONOCHROME LCD MONITOR is a medical device that received FDA 510(k) clearance on 2006-07-25. The listed applicant is Nec Display Solutions , Ltd.. The 510(k) number is K061947.

When did 21.3 INCH MONOCHROME LCD MONITOR receive FDA 510(k) clearance?

21.3 INCH MONOCHROME LCD MONITOR received FDA 510(k) clearance on 2006-07-25, under 510(k) number K061947.

Who is the listed applicant for 21.3 INCH MONOCHROME LCD MONITOR?

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 21.3 INCH MONOCHROME LCD MONITOR?

The FDA product code for 21.3 INCH MONOCHROME LCD MONITOR 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.

K161057Diagnostic Imaging Color LCD MonitorK130772MD211C2 21.3 DIAGNOSTIC IMAGING LCD MONITORK130770MD211C3 21.3 DIAGNOSTIC IMAGING LCD MONITORK111237MD301C4 29.8 DIAGNOSTIC IMAGING LCD MONITOR, L309TYK090218MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJK090215MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TL

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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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