Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDICAL DISPLAY, MD205MG

K-Number: K073448 · 2007-12-20

Decision Date2007-12-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDICAL DISPLAY, MD205MG is the device name listed in this FDA 510(k) record. The listed applicant is Nec Display Solutions , Ltd.. It received FDA 510(k) clearance on 2007-12-20 under 510(k) number K073448. 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, MD205MG?

MEDICAL DISPLAY, MD205MG is a medical device that received FDA 510(k) clearance on 2007-12-20. The listed applicant is Nec Display Solutions , Ltd.. The 510(k) number is K073448.

When did MEDICAL DISPLAY, MD205MG receive FDA 510(k) clearance?

MEDICAL DISPLAY, MD205MG received FDA 510(k) clearance on 2007-12-20, under 510(k) number K073448.

Who is the listed applicant for MEDICAL DISPLAY, MD205MG?

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

What is the FDA product code for MEDICAL DISPLAY, MD205MG?

The FDA product code for MEDICAL DISPLAY, MD205MG 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 Nec Display Solutions , 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 12 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.

↑