WET PLATINUM PERSONAL LUBRICANT
K-Number: K130012 · 2013-08-22
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Device Summary
Frequently Asked Questions
What is the WET PLATINUM PERSONAL LUBRICANT?
WET PLATINUM PERSONAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2013-08-22. The listed applicant is Trigg Laboratories, Inc.. The 510(k) number is K130012.
When did WET PLATINUM PERSONAL LUBRICANT receive FDA 510(k) clearance?
WET PLATINUM PERSONAL LUBRICANT received FDA 510(k) clearance on 2013-08-22, under 510(k) number K130012.
Who is the listed applicant for WET PLATINUM PERSONAL LUBRICANT?
The FDA 510(k) record lists Trigg Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WET PLATINUM PERSONAL LUBRICANT?
The FDA product code for WET PLATINUM PERSONAL LUBRICANT 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.
Other records listing Trigg Laboratories, Inc. as applicant
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
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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