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FDA 510(k)

PHARMAPAC PERSONAL LUBRICANT

K-Number: K091554 · 2009-08-07

Decision Date2009-08-07
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PHARMAPAC PERSONAL LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Pharmapac, LLC. It received FDA 510(k) clearance on 2009-08-07 under 510(k) number K091554. 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 PHARMAPAC PERSONAL LUBRICANT?

PHARMAPAC PERSONAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2009-08-07. The listed applicant is Pharmapac, LLC. The 510(k) number is K091554.

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

PHARMAPAC PERSONAL LUBRICANT received FDA 510(k) clearance on 2009-08-07, under 510(k) number K091554.

Who is the listed applicant for PHARMAPAC PERSONAL LUBRICANT?

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

What is the FDA product code for PHARMAPAC PERSONAL LUBRICANT?

The FDA product code for PHARMAPAC 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 Pharmapac, LLC 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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