PALMAZ XL TANSHEPATIC BILIARY STENTS
K-Number: K993091 · 1999-10-29
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Device Summary
Frequently Asked Questions
What is the PALMAZ XL TANSHEPATIC BILIARY STENTS?
PALMAZ XL TANSHEPATIC BILIARY STENTS is a medical device that received FDA 510(k) clearance on 1999-10-29. The listed applicant is Cordis Corp.. The 510(k) number is K993091.
When did PALMAZ XL TANSHEPATIC BILIARY STENTS receive FDA 510(k) clearance?
PALMAZ XL TANSHEPATIC BILIARY STENTS received FDA 510(k) clearance on 1999-10-29, under 510(k) number K993091.
Who is the listed applicant for PALMAZ XL TANSHEPATIC BILIARY STENTS?
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 PALMAZ XL TANSHEPATIC BILIARY STENTS?
The FDA product code for PALMAZ XL TANSHEPATIC BILIARY STENTS 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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