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FDA 510(k)

EXCELART VANTAGE ZGV

K-Number: K060003 · 2006-01-18

Decision Date2006-01-18
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EXCELART VANTAGE ZGV is the device name listed in this FDA 510(k) record. The listed applicant is Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2006-01-18 under 510(k) number K060003. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXCELART VANTAGE ZGV?

EXCELART VANTAGE ZGV is a medical device that received FDA 510(k) clearance on 2006-01-18. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K060003.

When did EXCELART VANTAGE ZGV receive FDA 510(k) clearance?

EXCELART VANTAGE ZGV received FDA 510(k) clearance on 2006-01-18, under 510(k) number K060003.

Who is the listed applicant for EXCELART VANTAGE ZGV?

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

What is the FDA product code for EXCELART VANTAGE ZGV?

The FDA product code for EXCELART VANTAGE ZGV is LNH.

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 Toshibamedical Systems 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 52 devices →

Related Devices (Code: LNH)

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.

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