BARD MEMOTHERM FLEXX BILIARY STENT
K-Number: K993392 · 2000-01-06
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Device Summary
Frequently Asked Questions
What is the BARD MEMOTHERM FLEXX BILIARY STENT?
BARD MEMOTHERM FLEXX BILIARY STENT is a medical device that received FDA 510(k) clearance on 2000-01-06. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K993392.
When did BARD MEMOTHERM FLEXX BILIARY STENT receive FDA 510(k) clearance?
BARD MEMOTHERM FLEXX BILIARY STENT received FDA 510(k) clearance on 2000-01-06, under 510(k) number K993392.
Who is the listed applicant for BARD MEMOTHERM FLEXX BILIARY STENT?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARD MEMOTHERM FLEXX BILIARY STENT?
The FDA product code for BARD MEMOTHERM FLEXX 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 C.R. Bard, 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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