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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 the device name listed in this FDA 510(k) record. The listed applicant is Good Clean Love, Inc.. It received FDA 510(k) clearance on 2021-11-18 under 510(k) 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. The listed applicant is Good Clean Love, Inc.. The 510(k) number is K211998.

When did Desnuda Reflect receive FDA 510(k) clearance?

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

Who is the listed applicant for Desnuda Reflect?

The FDA 510(k) record lists Good Clean Love, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Desnuda Reflect?

The FDA product code for Desnuda Reflect is NUC.

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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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