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FDA 510(k)

CloudVue

K-Number: K203058 · 2020-10-29

ApplicantInternational Medical Solutions, Inc.
Decision Date2020-10-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CloudVue is a medical device manufactured by International Medical Solutions, Inc.. It received FDA 510(k) clearance on 2020-10-29 under approval number K203058. 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 CloudVue?

CloudVue is a medical device that received FDA 510(k) clearance on 2020-10-29. It is manufactured by International Medical Solutions, Inc.. The 510(k) number is K203058.

When was CloudVue approved by the FDA?

CloudVue received FDA 510(k) clearance on 2020-10-29, under approval number K203058.

What company makes CloudVue?

CloudVue is manufactured by International Medical Solutions, Inc..

What is the FDA product code for CloudVue?

The FDA product code for CloudVue is LLZ.

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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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