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FDA 510(k)

DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT

K-Number: K072236 · 2008-05-07

ApplicantSsl Americas
Decision Date2008-05-07
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Ssl Americas. It received FDA 510(k) clearance on 2008-05-07 under 510(k) number K072236. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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