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FDA 510(k)

Sensual Massage, Ultra Pure

K-Number: K211967 · 2021-11-09

ApplicantDreambrands, Inc.
Decision Date2021-11-09
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Sensual Massage, Ultra Pure is a medical device manufactured by Dreambrands, Inc.. It received FDA 510(k) clearance on 2021-11-09 under approval number K211967. 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 Sensual Massage, Ultra Pure?

Sensual Massage, Ultra Pure is a medical device that received FDA 510(k) clearance on 2021-11-09. It is manufactured by Dreambrands, Inc.. The 510(k) number is K211967.

When was Sensual Massage, Ultra Pure approved by the FDA?

Sensual Massage, Ultra Pure received FDA 510(k) clearance on 2021-11-09, under approval number K211967.

What company makes Sensual Massage, Ultra Pure?

Sensual Massage, Ultra Pure is manufactured by Dreambrands, Inc..

What is the FDA product code for Sensual Massage, Ultra Pure?

The FDA product code for Sensual Massage, Ultra Pure is NUC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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