MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM
K-Number: K032530 · 2003-10-23
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM?
MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-23. The listed applicant is Guidant Corporation. The 510(k) number is K032530.
When did MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM receive FDA 510(k) clearance?
MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM received FDA 510(k) clearance on 2003-10-23, under 510(k) number K032530.
Who is the listed applicant for MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM?
The FDA 510(k) record lists Guidant Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM?
The FDA product code for MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM 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 Guidant Corporation 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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