PHARMAPAC LUBRICATING JELLY
K-Number: K070623 · 2007-08-31
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Device Summary
Frequently Asked Questions
What is the PHARMAPAC LUBRICATING JELLY?
PHARMAPAC LUBRICATING JELLY is a medical device that received FDA 510(k) clearance on 2007-08-31. The listed applicant is Pharmapac, LLC. The 510(k) number is K070623.
When did PHARMAPAC LUBRICATING JELLY receive FDA 510(k) clearance?
PHARMAPAC LUBRICATING JELLY received FDA 510(k) clearance on 2007-08-31, under 510(k) number K070623.
Who is the listed applicant for PHARMAPAC LUBRICATING JELLY?
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 LUBRICATING JELLY?
The FDA product code for PHARMAPAC LUBRICATING JELLY 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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