AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
PMA Number: P000029 · 2024-05-31
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Device Summary
Frequently Asked Questions
What is the AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE?
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE is a medical device that received FDA 510(k) clearance on 2024-05-31. The listed applicant is Palette Life Sciences.
When did AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE receive FDA 510(k) clearance?
The clearance date for AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE can be found in the official FDA records.
Who is the listed applicant for AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE?
The FDA 510(k) record lists Palette Life Sciences as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE?
The FDA product code for AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE is LNM.
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.
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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