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FDA 510(k)

Multi Modality Viewer

K-Number: K163574 · 2017-01-26

ApplicantVital Images, Inc.
Decision Date2017-01-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Multi Modality Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Vital Images, Inc.. It received FDA 510(k) clearance on 2017-01-26 under 510(k) number K163574. 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 2017-01-26. The listed applicant is Vital Images, Inc.. The 510(k) number is K163574.

When did Multi Modality Viewer receive FDA 510(k) clearance?

Multi Modality Viewer received FDA 510(k) clearance on 2017-01-26, under 510(k) number K163574.

Who is the listed applicant for Multi Modality Viewer?

The FDA 510(k) record lists Vital Images, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multi Modality Viewer?

The FDA product code for Multi Modality Viewer is LLZ.

Other records listing Vital Images, Inc. as applicant

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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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