FDA 510(k)

Revaree Plus Vaginal Suppositories

K-Number: K213220 · 2022-06-21

Decision Date2022-06-21

Product CodeNUC

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

Revaree Plus Vaginal Suppositories is a medical device manufactured by Farma-Derma S.R.L.. It received FDA 510(k) clearance on 2022-06-21 under approval number K213220. 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 Revaree Plus Vaginal Suppositories?

Revaree Plus Vaginal Suppositories is a medical device that received FDA 510(k) clearance on 2022-06-21. It is manufactured by Farma-Derma S.R.L.. The 510(k) number is K213220.

When was Revaree Plus Vaginal Suppositories approved by the FDA?

Revaree Plus Vaginal Suppositories received FDA 510(k) clearance on 2022-06-21, under approval number K213220.

What company makes Revaree Plus Vaginal Suppositories?

Revaree Plus Vaginal Suppositories is manufactured by Farma-Derma S.R.L..

What is the FDA product code for Revaree Plus Vaginal Suppositories?

The FDA product code for Revaree Plus Vaginal Suppositories is NUC.

Other Devices by Farma-Derma S.R.L.

K153372Repagyn vaginal suppositories

Related Devices (Code: NUC)

K161585Mano and Mano Personal LubricantMano and Mano Proprietary Limited K161544Trojan Chain Reaction Personal LubricantChurch & Dwight Co., Inc. K161385Just Like Me Personal LubricantWtfn-Dba Classic Erotica/Holiday Products K152671Pulse Aloe-ahhToaster Labs, Inc. K152628Pulse H20h!Toaster Labs, Inc. K153372Repagyn vaginal suppositoriesFarma-Derma S.R.L.

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.