PRE-VA VAGINAL LUBRICANT
K-Number: K072741 · 2008-07-16
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Device Summary
Frequently Asked Questions
What is the PRE-VA VAGINAL LUBRICANT?
PRE-VA VAGINAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2008-07-16. The listed applicant is Ingfertility, LLC. The 510(k) number is K072741.
When did PRE-VA VAGINAL LUBRICANT receive FDA 510(k) clearance?
PRE-VA VAGINAL LUBRICANT received FDA 510(k) clearance on 2008-07-16, under 510(k) number K072741.
Who is the listed applicant for PRE-VA VAGINAL LUBRICANT?
The FDA 510(k) record lists Ingfertility, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRE-VA VAGINAL LUBRICANT?
The FDA product code for PRE-VA VAGINAL LUBRICANT is PEB.
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: PEB)
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
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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