DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT
K-Number: K072236 · 2008-05-07
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Device Summary
Frequently Asked Questions
What is the DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT?
DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT is a medical device that received FDA 510(k) clearance on 2008-05-07. The listed applicant is Ssl Americas. The 510(k) number is K072236.
When did DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT receive FDA 510(k) clearance?
DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT received FDA 510(k) clearance on 2008-05-07, under 510(k) number K072236.
Who is the listed applicant for DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT?
The FDA 510(k) record lists Ssl Americas as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT?
The FDA product code for DUREX PLAY TINGLING AQUEOUS BASED 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 Ssl Americas 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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