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FDA 510(k)

Visura Technologies TEECAD System

K-Number: K180911 · 2018-06-20

ApplicantVisura Technologies, LLC
Decision Date2018-06-20
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Visura Technologies TEECAD System is a medical device manufactured by Visura Technologies, LLC. It received FDA 510(k) clearance on 2018-06-20 under approval number K180911. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Visura Technologies TEECAD System?

Visura Technologies TEECAD System is a medical device that received FDA 510(k) clearance on 2018-06-20. It is manufactured by Visura Technologies, LLC. The 510(k) number is K180911.

When was Visura Technologies TEECAD System approved by the FDA?

Visura Technologies TEECAD System received FDA 510(k) clearance on 2018-06-20, under approval number K180911.

What company makes Visura Technologies TEECAD System?

Visura Technologies TEECAD System is manufactured by Visura Technologies, LLC.

What is the FDA product code for Visura Technologies TEECAD System?

The FDA product code for Visura Technologies TEECAD System is FDS.

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Related PubMed Literature

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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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