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 the device name listed in this FDA 510(k) record. The listed applicant is International Medical Solutions, Inc.. It received FDA 510(k) clearance on 2020-10-29 under 510(k) 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. The listed applicant is International Medical Solutions, Inc.. The 510(k) number is K203058.

When did CloudVue receive FDA 510(k) clearance?

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

Who is the listed applicant for CloudVue?

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

What is the FDA product code for CloudVue?

The FDA product code for CloudVue is LLZ.

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLC K261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific Corporation K262143ImageGrid StreamVueCandelis, Inc.

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.