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FDA 510(k)

CVS PERSONAL LUBRICANT AND MOISTURIZER

K-Number: K062682 · 2007-04-04

Decision Date2007-04-04
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CVS PERSONAL LUBRICANT AND MOISTURIZER is the device name listed in this FDA 510(k) record. The listed applicant is Lake Consumer Products, Inc.. It received FDA 510(k) clearance on 2007-04-04 under 510(k) number K062682. 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 CVS PERSONAL LUBRICANT AND MOISTURIZER?

CVS PERSONAL LUBRICANT AND MOISTURIZER is a medical device that received FDA 510(k) clearance on 2007-04-04. The listed applicant is Lake Consumer Products, Inc.. The 510(k) number is K062682.

When did CVS PERSONAL LUBRICANT AND MOISTURIZER receive FDA 510(k) clearance?

CVS PERSONAL LUBRICANT AND MOISTURIZER received FDA 510(k) clearance on 2007-04-04, under 510(k) number K062682.

Who is the listed applicant for CVS PERSONAL LUBRICANT AND MOISTURIZER?

The FDA 510(k) record lists Lake Consumer Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CVS PERSONAL LUBRICANT AND MOISTURIZER?

The FDA product code for CVS PERSONAL LUBRICANT AND MOISTURIZER is NUC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: NUC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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