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FDA 510(k)

VANTAGE TITAN 3T

K-Number: K102489 · 2011-08-02

Decision Date2011-08-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VANTAGE TITAN 3T is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems Corporation, Japan. It received FDA 510(k) clearance on 2011-08-02 under 510(k) number K102489. 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 VANTAGE TITAN 3T?

VANTAGE TITAN 3T is a medical device that received FDA 510(k) clearance on 2011-08-02. The listed applicant is Toshiba Medical Systems Corporation, Japan. The 510(k) number is K102489.

When did VANTAGE TITAN 3T receive FDA 510(k) clearance?

VANTAGE TITAN 3T received FDA 510(k) clearance on 2011-08-02, under 510(k) number K102489.

Who is the listed applicant for VANTAGE TITAN 3T?

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

What is the FDA product code for VANTAGE TITAN 3T?

The FDA product code for VANTAGE TITAN 3T 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 Toshiba Medical Systems Corporation, Japan 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.

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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

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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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