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FDA 510(k)

VANTAGE TITAN, MODEL MRT-1504/S3

K-Number: K080038 · 2008-01-22

ApplicantToshiba America Medical Systems, In.C
Decision Date2008-01-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VANTAGE TITAN, MODEL MRT-1504/S3 is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 2008-01-22 under 510(k) number K080038. 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, MODEL MRT-1504/S3?

VANTAGE TITAN, MODEL MRT-1504/S3 is a medical device that received FDA 510(k) clearance on 2008-01-22. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K080038.

When did VANTAGE TITAN, MODEL MRT-1504/S3 receive FDA 510(k) clearance?

VANTAGE TITAN, MODEL MRT-1504/S3 received FDA 510(k) clearance on 2008-01-22, under 510(k) number K080038.

Who is the listed applicant for VANTAGE TITAN, MODEL MRT-1504/S3?

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

What is the FDA product code for VANTAGE TITAN, MODEL MRT-1504/S3?

The FDA product code for VANTAGE TITAN, MODEL MRT-1504/S3 is LNH.

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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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