PHARMAPAC PERSONAL LUBRICANT
K-Number: K091554 · 2009-08-07
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Device Summary
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
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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