Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Personal Lubricant

K-Number: K210857 · 2021-09-24

ApplicantShenzhen Huanqiu Xuebao Technology Co., Ltd.
Decision Date2021-09-24
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Personal Lubricant is a medical device manufactured by Shenzhen Huanqiu Xuebao Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-09-24 under approval number K210857. 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 Personal Lubricant?

Personal Lubricant is a medical device that received FDA 510(k) clearance on 2021-09-24. It is manufactured by Shenzhen Huanqiu Xuebao Technology Co., Ltd.. The 510(k) number is K210857.

When was Personal Lubricant approved by the FDA?

Personal Lubricant received FDA 510(k) clearance on 2021-09-24, under approval number K210857.

What company makes Personal Lubricant?

Personal Lubricant is manufactured by Shenzhen Huanqiu Xuebao Technology Co., Ltd..

What is the FDA product code for Personal Lubricant?

The FDA product code for Personal Lubricant is NUC.

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

View on FDA Database →

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

↑