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FDA 510(k)

Multi Modality Viewer

K-Number: K182230 · 2018-09-07

ApplicantVital Images, Inc.
Decision Date2018-09-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Multi Modality Viewer is a medical device manufactured by Vital Images, Inc.. It received FDA 510(k) clearance on 2018-09-07 under approval number K182230. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Multi Modality Viewer?

Multi Modality Viewer is a medical device that received FDA 510(k) clearance on 2018-09-07. It is manufactured by Vital Images, Inc.. The 510(k) number is K182230.

When was Multi Modality Viewer approved by the FDA?

Multi Modality Viewer received FDA 510(k) clearance on 2018-09-07, under approval number K182230.

What company makes Multi Modality Viewer?

Multi Modality Viewer is manufactured by Vital Images, Inc..

What is the FDA product code for Multi Modality Viewer?

The FDA product code for Multi Modality Viewer is LLZ.

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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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