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)

COLOR LCD MONITOR, FLEXSCAN MX300W

K-Number: K073340 · 2007-12-19

Decision Date2007-12-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLOR LCD MONITOR, FLEXSCAN MX300W is the device name listed in this FDA 510(k) record. The listed applicant is Eizo Nanao Corporation. It received FDA 510(k) clearance on 2007-12-19 under 510(k) number K073340. 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 COLOR LCD MONITOR, FLEXSCAN MX300W?

COLOR LCD MONITOR, FLEXSCAN MX300W is a medical device that received FDA 510(k) clearance on 2007-12-19. The listed applicant is Eizo Nanao Corporation. The 510(k) number is K073340.

When did COLOR LCD MONITOR, FLEXSCAN MX300W receive FDA 510(k) clearance?

COLOR LCD MONITOR, FLEXSCAN MX300W received FDA 510(k) clearance on 2007-12-19, under 510(k) number K073340.

Who is the listed applicant for COLOR LCD MONITOR, FLEXSCAN MX300W?

The FDA 510(k) record lists Eizo Nanao Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLOR LCD MONITOR, FLEXSCAN MX300W?

The FDA product code for COLOR LCD MONITOR, FLEXSCAN MX300W 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 Eizo Nanao Corporation 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 34 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.

↑