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FDA 510(k)

Cornisol

K-Number: K221759 · 2022-10-05

ApplicantAurolab
Decision Date2022-10-05
Product CodeLYX
DecisionSubstantially Equivalent

Device Summary

Cornisol is a medical device manufactured by Aurolab. It received FDA 510(k) clearance on 2022-10-05 under approval number K221759. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cornisol?

Cornisol is a medical device that received FDA 510(k) clearance on 2022-10-05. It is manufactured by Aurolab. The 510(k) number is K221759.

When was Cornisol approved by the FDA?

Cornisol received FDA 510(k) clearance on 2022-10-05, under approval number K221759.

What company makes Cornisol?

Cornisol is manufactured by Aurolab.

What is the FDA product code for Cornisol?

The FDA product code for Cornisol is LYX.

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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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