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FDA 510(k)

VISART

K-Number: K961092 · 1996-06-14

ApplicantToshiba America Medical Systems, In.C
Decision Date1996-06-14
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISART 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 1996-06-14 under 510(k) number K961092. 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 VISART?

VISART is a medical device that received FDA 510(k) clearance on 1996-06-14. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K961092.

When did VISART receive FDA 510(k) clearance?

VISART received FDA 510(k) clearance on 1996-06-14, under 510(k) number K961092.

Who is the listed applicant for VISART?

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 VISART?

The FDA product code for VISART 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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