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FDA 510(k)

FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES

K-Number: K021738 · 2002-08-19

ApplicantTotoku Electric Co., Ltd.
Decision Date2002-08-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Totoku Electric Co., Ltd.. It received FDA 510(k) clearance on 2002-08-19 under 510(k) number K021738. 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 FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES?

FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES is a medical device that received FDA 510(k) clearance on 2002-08-19. The listed applicant is Totoku Electric Co., Ltd.. The 510(k) number is K021738.

When did FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES receive FDA 510(k) clearance?

FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES received FDA 510(k) clearance on 2002-08-19, under 510(k) number K021738.

Who is the listed applicant for FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES?

The FDA 510(k) record lists Totoku Electric Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES?

The FDA product code for FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES is 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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