CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT
K-Number: K012090 · 2001-08-01
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Device Summary
Frequently Asked Questions
What is the CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT?
CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT is a medical device that received FDA 510(k) clearance on 2001-08-01. The listed applicant is Cordis, A Johnson & Johnson Co.. The 510(k) number is K012090.
When did CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT receive FDA 510(k) clearance?
CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT received FDA 510(k) clearance on 2001-08-01, under 510(k) number K012090.
Who is the listed applicant for CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT?
The FDA 510(k) record lists Cordis, A Johnson & Johnson Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT?
The FDA product code for CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT 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, A Johnson & Johnson Co. 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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