FDA 510(k)

INDIRA CLOUD VIEWER

K-Number: K261465 · 2026-07-06

Decision Date2026-07-06

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

INDIRA CLOUD VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is INDIGO TECHNOLOGIES. It received FDA 510(k) clearance on 2026-07-06 under 510(k) number K261465. 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 INDIRA CLOUD VIEWER?

INDIRA CLOUD VIEWER is a medical device that received FDA 510(k) clearance on 2026-07-06. The listed applicant is INDIGO TECHNOLOGIES. The 510(k) number is K261465.

When did INDIRA CLOUD VIEWER receive FDA 510(k) clearance?

INDIRA CLOUD VIEWER received FDA 510(k) clearance on 2026-07-06, under 510(k) number K261465.

Who is the listed applicant for INDIRA CLOUD VIEWER?

The FDA 510(k) record lists INDIGO TECHNOLOGIES as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INDIRA CLOUD VIEWER?

The FDA product code for INDIRA CLOUD VIEWER 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.