FDA 510(k)

Revaree Plus Vaginal Suppositories

K号: K213220 · 2022-06-21

决定日期2022-06-21

产品代码NUC

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决定实质等同

器械摘要

Revaree Plus Vaginal Suppositories is the device name listed in this FDA 510(k) record. The listed applicant is Farma-Derma S.R.L.. It received FDA 510(k) clearance on 2022-06-21 under 510(k) number K213220. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

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. The listed applicant is Farma-Derma S.R.L.. The 510(k) number is K213220.

When did Revaree Plus Vaginal Suppositories receive FDA 510(k) clearance?

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

Who is the listed applicant for Revaree Plus Vaginal Suppositories?

The FDA 510(k) record lists Farma-Derma S.R.L. as the applicant. This does not by itself establish the device manufacturer.

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

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

列明Farma-Derma S.R.L.为申报人的其他记录

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