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FDA 510(k)

ClariCT.AI

K-Number: K212074 · 2021-07-27

ApplicantClaripi, Inc.
Decision Date2021-07-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ClariCT.AI is a medical device manufactured by Claripi, Inc.. It received FDA 510(k) clearance on 2021-07-27 under approval number K212074. 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 ClariCT.AI?

ClariCT.AI is a medical device that received FDA 510(k) clearance on 2021-07-27. It is manufactured by Claripi, Inc.. The 510(k) number is K212074.

When was ClariCT.AI approved by the FDA?

ClariCT.AI received FDA 510(k) clearance on 2021-07-27, under approval number K212074.

What company makes ClariCT.AI?

ClariCT.AI is manufactured by Claripi, Inc..

What is the FDA product code for ClariCT.AI?

The FDA product code for ClariCT.AI is LLZ.

Other Devices by Claripi, Inc.

K183460ClariCT.AI K203785ClariSIGMAM K203783ClariPulmo

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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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