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FDA 510(k)

2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC

K-Number: K063579 · 2006-12-14

Decision Date2006-12-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC is the device name listed in this FDA 510(k) record. The listed applicant is Chi Lin Technology Co., Ltd.. It received FDA 510(k) clearance on 2006-12-14 under 510(k) number K063579. 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 2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC?

2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC is a medical device that received FDA 510(k) clearance on 2006-12-14. The listed applicant is Chi Lin Technology Co., Ltd.. The 510(k) number is K063579.

When did 2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC receive FDA 510(k) clearance?

2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC received FDA 510(k) clearance on 2006-12-14, under 510(k) number K063579.

Who is the listed applicant for 2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC?

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

What is the FDA product code for 2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC?

The FDA product code for 2MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HC 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 Chi Lin Technology 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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