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FDA 510(k)

MEDICAL DISPLAY, MODELS MDM 1900-1NG AND MDM 1900-1NR

K-Number: K061303 · 2006-05-25

Decision Date2006-05-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDICAL DISPLAY, MODELS MDM 1900-1NG AND MDM 1900-1NR 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 K061303. 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, MODELS MDM 1900-1NG AND MDM 1900-1NR?

MEDICAL DISPLAY, MODELS MDM 1900-1NG AND MDM 1900-1NR 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 K061303.

When did MEDICAL DISPLAY, MODELS MDM 1900-1NG AND MDM 1900-1NR receive FDA 510(k) clearance?

MEDICAL DISPLAY, MODELS MDM 1900-1NG AND MDM 1900-1NR received FDA 510(k) clearance on 2006-05-25, under 510(k) number K061303.

Who is the listed applicant for MEDICAL DISPLAY, MODELS MDM 1900-1NG AND MDM 1900-1NR?

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, MODELS MDM 1900-1NG AND MDM 1900-1NR?

The FDA product code for MEDICAL DISPLAY, MODELS MDM 1900-1NG AND MDM 1900-1NR 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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