ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER
K-Number: K002101 · 2000-07-31
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Device Summary
Frequently Asked Questions
What is the ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER?
ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER is a medical device that received FDA 510(k) clearance on 2000-07-31. The listed applicant is AngioDynamics, Inc.. The 510(k) number is K002101.
When did ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER receive FDA 510(k) clearance?
ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER received FDA 510(k) clearance on 2000-07-31, under 510(k) number K002101.
Who is the listed applicant for ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER?
The FDA 510(k) record lists AngioDynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER?
The FDA product code for ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER 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 AngioDynamics, Inc. 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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