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FDA 510(k)

Desnuda Reflect

K-Number: K211998 · 2021-11-18

ApplicantGood Clean Love, Inc.
Decision Date2021-11-18
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Desnuda Reflect is a medical device manufactured by Good Clean Love, Inc.. It received FDA 510(k) clearance on 2021-11-18 under approval number K211998. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Desnuda Reflect?

Desnuda Reflect is a medical device that received FDA 510(k) clearance on 2021-11-18. It is manufactured by Good Clean Love, Inc.. The 510(k) number is K211998.

When was Desnuda Reflect approved by the FDA?

Desnuda Reflect received FDA 510(k) clearance on 2021-11-18, under approval number K211998.

What company makes Desnuda Reflect?

Desnuda Reflect is manufactured by Good Clean Love, Inc..

What is the FDA product code for Desnuda Reflect?

The FDA product code for Desnuda Reflect is NUC.

Other Devices by Good Clean Love, Inc.

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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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