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FDA 510(k)

FLAT PANEL DISPLAYS, CDL SERIES

K-Number: K030276 · 2003-04-25

Decision Date2003-04-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLAT PANEL DISPLAYS, CDL 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 2003-04-25 under 510(k) number K030276. 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, CDL SERIES?

FLAT PANEL DISPLAYS, CDL SERIES is a medical device that received FDA 510(k) clearance on 2003-04-25. The listed applicant is Totoku Electric Co., Ltd.. The 510(k) number is K030276.

When did FLAT PANEL DISPLAYS, CDL SERIES receive FDA 510(k) clearance?

FLAT PANEL DISPLAYS, CDL SERIES received FDA 510(k) clearance on 2003-04-25, under 510(k) number K030276.

Who is the listed applicant for FLAT PANEL DISPLAYS, CDL 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, CDL SERIES?

The FDA product code for FLAT PANEL DISPLAYS, CDL SERIES 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 Totoku Electric Co., 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)

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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