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FDA 510(k)

NIRVANA B PERSONAL LUBRICANT

K-Number: K120751 · 2012-10-03

Decision Date2012-10-03
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NIRVANA B PERSONAL LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Church & Dwight Co., Inc.. It received FDA 510(k) clearance on 2012-10-03 under 510(k) number K120751. 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 NIRVANA B PERSONAL LUBRICANT?

NIRVANA B PERSONAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2012-10-03. The listed applicant is Church & Dwight Co., Inc.. The 510(k) number is K120751.

When did NIRVANA B PERSONAL LUBRICANT receive FDA 510(k) clearance?

NIRVANA B PERSONAL LUBRICANT received FDA 510(k) clearance on 2012-10-03, under 510(k) number K120751.

Who is the listed applicant for NIRVANA B PERSONAL LUBRICANT?

The FDA 510(k) record lists Church & Dwight Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIRVANA B PERSONAL LUBRICANT?

The FDA product code for NIRVANA B 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 Church & Dwight Co., 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.

View all 27 devices →

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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