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FDA 510(k)

20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2)

K-Number: K072065 · 2007-08-14

Decision Date2007-08-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2) 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 2007-08-14 under 510(k) number K072065. 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 20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2)?

20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2) is a medical device that received FDA 510(k) clearance on 2007-08-14. The listed applicant is Totoku Electric Co., Ltd.. The 510(k) number is K072065.

When did 20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2) receive FDA 510(k) clearance?

20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2) received FDA 510(k) clearance on 2007-08-14, under 510(k) number K072065.

Who is the listed applicant for 20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2)?

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 20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2)?

The FDA product code for 20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2) 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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