FDA 510(k)

FDS INTIMATE AND INTIMATE WARMING LUBRICANT

K-Number: K060145 · 2006-04-14

Decision Date2006-04-14

Product CodeNUC

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

FDS INTIMATE AND INTIMATE WARMING LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Alberto-Culver USA, Inc.. It received FDA 510(k) clearance on 2006-04-14 under 510(k) number K060145. 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 FDS INTIMATE AND INTIMATE WARMING LUBRICANT?

FDS INTIMATE AND INTIMATE WARMING LUBRICANT is a medical device that received FDA 510(k) clearance on 2006-04-14. The listed applicant is Alberto-Culver USA, Inc.. The 510(k) number is K060145.

When did FDS INTIMATE AND INTIMATE WARMING LUBRICANT receive FDA 510(k) clearance?

FDS INTIMATE AND INTIMATE WARMING LUBRICANT received FDA 510(k) clearance on 2006-04-14, under 510(k) number K060145.

Who is the listed applicant for FDS INTIMATE AND INTIMATE WARMING LUBRICANT?

The FDA 510(k) record lists Alberto-Culver USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FDS INTIMATE AND INTIMATE WARMING LUBRICANT?

The FDA product code for FDS INTIMATE AND INTIMATE WARMING LUBRICANT is NUC.

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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.