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FDA 510(k)

MEDICAL DISPLAY, MDC1900-1LG (1LR)

K-Number: K061305 · 2006-05-25

ApplicantChi Lin Technology Co., Ltd.
Decision Date2006-05-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDICAL DISPLAY, MDC1900-1LG (1LR) 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 2006-05-25 under 510(k) number K061305. 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 MEDICAL DISPLAY, MDC1900-1LG (1LR)?

MEDICAL DISPLAY, MDC1900-1LG (1LR) is a medical device that received FDA 510(k) clearance on 2006-05-25. The listed applicant is Chi Lin Technology Co., Ltd.. The 510(k) number is K061305.

When did MEDICAL DISPLAY, MDC1900-1LG (1LR) receive FDA 510(k) clearance?

MEDICAL DISPLAY, MDC1900-1LG (1LR) received FDA 510(k) clearance on 2006-05-25, under 510(k) number K061305.

Who is the listed applicant for MEDICAL DISPLAY, MDC1900-1LG (1LR)?

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 MEDICAL DISPLAY, MDC1900-1LG (1LR)?

The FDA product code for MEDICAL DISPLAY, MDC1900-1LG (1LR) is LLZ.

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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.

K0632695MP MEDICAL MONOCHROME REFERENCE DISPLAY, MODEL MDM2010-5NCK0635792MP MEDICAL COLOR REFERENCE DISPLAY, MODEL MDC2130-2HCK0632892MP MEDICAL MONOCHROME REFERENCE DISPLAY, MODEL MDM2130-2NCK0632663MP MEDICAL MONOCHROME REFERENCE DISPLAY, MODEL MDM2130-3NCK061303MEDICAL DISPLAY, MODELS MDM 1900-1NG AND MDM 1900-1NR

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.

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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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