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FDA 510(k)

Climax Personal Lubricant

K-Number: K171044 · 2017-11-21

ApplicantWsm Investment, LLC, Dba Topco Sales
Decision Date2017-11-21
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Climax Personal Lubricant is a medical device manufactured by Wsm Investment, LLC, Dba Topco Sales. It received FDA 510(k) clearance on 2017-11-21 under approval number K171044. 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 Climax Personal Lubricant?

Climax Personal Lubricant is a medical device that received FDA 510(k) clearance on 2017-11-21. It is manufactured by Wsm Investment, LLC, Dba Topco Sales. The 510(k) number is K171044.

When was Climax Personal Lubricant approved by the FDA?

Climax Personal Lubricant received FDA 510(k) clearance on 2017-11-21, under approval number K171044.

What company makes Climax Personal Lubricant?

Climax Personal Lubricant is manufactured by Wsm Investment, LLC, Dba Topco Sales.

What is the FDA product code for Climax Personal Lubricant?

The FDA product code for Climax Personal Lubricant is NUC.

Related Devices (Code: 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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