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FDA 510(k)

WARMING JELLY PERSONAL LUBRICANT

K-Number: K123770 · 2013-04-09

Decision Date2013-04-09
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WARMING JELLY PERSONAL LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Wisconsin Pharmacal Co., LLC. It received FDA 510(k) clearance on 2013-04-09 under 510(k) number K123770. 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 WARMING JELLY PERSONAL LUBRICANT?

WARMING JELLY PERSONAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2013-04-09. The listed applicant is Wisconsin Pharmacal Co., LLC. The 510(k) number is K123770.

When did WARMING JELLY PERSONAL LUBRICANT receive FDA 510(k) clearance?

WARMING JELLY PERSONAL LUBRICANT received FDA 510(k) clearance on 2013-04-09, under 510(k) number K123770.

Who is the listed applicant for WARMING JELLY PERSONAL LUBRICANT?

The FDA 510(k) record lists Wisconsin Pharmacal Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WARMING JELLY PERSONAL LUBRICANT?

The FDA product code for WARMING JELLY 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.

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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