DUREX PLAY TINGLING LUBRICANT
K-Number: K042958 · 2005-04-08
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Device Summary
Frequently Asked Questions
What is the DUREX PLAY TINGLING LUBRICANT?
DUREX PLAY TINGLING LUBRICANT is a medical device that received FDA 510(k) clearance on 2005-04-08. The listed applicant is Ssl Americas, Inc.. The 510(k) number is K042958.
When did DUREX PLAY TINGLING LUBRICANT receive FDA 510(k) clearance?
DUREX PLAY TINGLING LUBRICANT received FDA 510(k) clearance on 2005-04-08, under 510(k) number K042958.
Who is the listed applicant for DUREX PLAY TINGLING LUBRICANT?
The FDA 510(k) record lists Ssl Americas, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUREX PLAY TINGLING LUBRICANT?
The FDA product code for DUREX PLAY TINGLING 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, 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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