NAVARRE PERCUTANEOUS BILIARY DRAINAGE
K-Number: K955110 · 1996-11-07
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Device Summary
Frequently Asked Questions
What is the NAVARRE PERCUTANEOUS BILIARY DRAINAGE?
NAVARRE PERCUTANEOUS BILIARY DRAINAGE is a medical device that received FDA 510(k) clearance on 1996-11-07. The listed applicant is Navarre Biomedical , Ltd.. The 510(k) number is K955110.
When did NAVARRE PERCUTANEOUS BILIARY DRAINAGE receive FDA 510(k) clearance?
NAVARRE PERCUTANEOUS BILIARY DRAINAGE received FDA 510(k) clearance on 1996-11-07, under 510(k) number K955110.
Who is the listed applicant for NAVARRE PERCUTANEOUS BILIARY DRAINAGE?
The FDA 510(k) record lists Navarre Biomedical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NAVARRE PERCUTANEOUS BILIARY DRAINAGE?
The FDA product code for NAVARRE PERCUTANEOUS BILIARY DRAINAGE is FGE.
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 Navarre Biomedical , Ltd. 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: FGE)
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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