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FDA 510(k)

PRE' VAGINAL LUBRICANT

K-Number: K051436 · 2006-10-13

ApplicantIngfertlity, LLC
Decision Date2006-10-13
Product CodePEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PRE' VAGINAL LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Ingfertlity, LLC. It received FDA 510(k) clearance on 2006-10-13 under 510(k) number K051436. The device is classified under product code PEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE' VAGINAL LUBRICANT?

PRE' VAGINAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2006-10-13. The listed applicant is Ingfertlity, LLC. The 510(k) number is K051436.

When did PRE' VAGINAL LUBRICANT receive FDA 510(k) clearance?

PRE' VAGINAL LUBRICANT received FDA 510(k) clearance on 2006-10-13, under 510(k) number K051436.

Who is the listed applicant for PRE' VAGINAL LUBRICANT?

The FDA 510(k) record lists Ingfertlity, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRE' VAGINAL LUBRICANT?

The FDA product code for PRE' VAGINAL LUBRICANT is PEB.

Related Clinical Trials

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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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