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FDA 510(k)

LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50

K-Number: K052120 · 2005-12-16

Decision Date2005-12-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50 is the device name listed in this FDA 510(k) record. The listed applicant is Heeyoung Co., Ltd.. It received FDA 510(k) clearance on 2005-12-16 under 510(k) number K052120. 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 LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50?

LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50 is a medical device that received FDA 510(k) clearance on 2005-12-16. The listed applicant is Heeyoung Co., Ltd.. The 510(k) number is K052120.

When did LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50 receive FDA 510(k) clearance?

LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50 received FDA 510(k) clearance on 2005-12-16, under 510(k) number K052120.

Who is the listed applicant for LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50?

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

What is the FDA product code for LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50?

The FDA product code for LUMIMED MONOCHROME LCD MONITOR, MODELS MM 20, MM 30 AND MM50 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 Heeyoung 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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