S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
K-Number: K994068 · 1999-12-23
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Device Summary
Frequently Asked Questions
What is the S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM?
S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM is a medical device that received FDA 510(k) clearance on 1999-12-23. The listed applicant is Cordis Corp.. The 510(k) number is K994068.
When did S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM receive FDA 510(k) clearance?
S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM received FDA 510(k) clearance on 1999-12-23, under 510(k) number K994068.
Who is the listed applicant for S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM?
The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY SYSTEM?
The FDA product code for S.M.A.R.T. NITINOL STENT TRANSHEPATIC BILIARY 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 Cordis Corp. 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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