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FDA 510(k)

Nu Skin RenuSpa iO

K-Number: K232001 · 2023-11-21

ApplicantNse Products, Inc.
Decision Date2023-11-21
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Nu Skin RenuSpa iO is a medical device manufactured by Nse Products, Inc.. It received FDA 510(k) clearance on 2023-11-21 under approval number K232001. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nu Skin RenuSpa iO?

Nu Skin RenuSpa iO is a medical device that received FDA 510(k) clearance on 2023-11-21. It is manufactured by Nse Products, Inc.. The 510(k) number is K232001.

When was Nu Skin RenuSpa iO approved by the FDA?

Nu Skin RenuSpa iO received FDA 510(k) clearance on 2023-11-21, under approval number K232001.

What company makes Nu Skin RenuSpa iO?

Nu Skin RenuSpa iO is manufactured by Nse Products, Inc..

What is the FDA product code for Nu Skin RenuSpa iO?

The FDA product code for Nu Skin RenuSpa iO is NFO.

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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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