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FDA 510(k)

21.3-INCH (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2)

K-Number: K063199 · 2006-12-04

Decision Date2006-12-04
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

21.3-INCH (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2) 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 2006-12-04 under 510(k) number K063199. 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 (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2)?

21.3-INCH (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2) is a medical device that received FDA 510(k) clearance on 2006-12-04. The listed applicant is Totoku Electric Co., Ltd.. The 510(k) number is K063199.

When did 21.3-INCH (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2) receive FDA 510(k) clearance?

21.3-INCH (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2) received FDA 510(k) clearance on 2006-12-04, under 510(k) number K063199.

Who is the listed applicant for 21.3-INCH (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2)?

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 21.3-INCH (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2)?

The FDA product code for 21.3-INCH (54CM) COLOR LCD MONITOR CDL2120A (CCL252I2) 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.

View all 40 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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