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FDA 510(k)

VCF PERSONAL LUBRICANT

K-Number: K010182 · 2001-03-09

Decision Date2001-03-09
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VCF PERSONAL LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Apothecus Pharmaceutical Corp.. It received FDA 510(k) clearance on 2001-03-09 under 510(k) number K010182. 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 VCF PERSONAL LUBRICANT?

VCF PERSONAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2001-03-09. The listed applicant is Apothecus Pharmaceutical Corp.. The 510(k) number is K010182.

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

VCF PERSONAL LUBRICANT received FDA 510(k) clearance on 2001-03-09, under 510(k) number K010182.

Who is the listed applicant for VCF PERSONAL LUBRICANT?

The FDA 510(k) record lists Apothecus Pharmaceutical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VCF PERSONAL LUBRICANT?

The FDA product code for VCF 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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