BARD CONFORMEXX BILIARY STENT WITH THE PERFORMAXX GRIP
K-Number: K052114 · 2005-08-25
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Device Summary
Frequently Asked Questions
What is the BARD CONFORMEXX BILIARY STENT WITH THE PERFORMAXX GRIP?
BARD CONFORMEXX BILIARY STENT WITH THE PERFORMAXX GRIP is a medical device that received FDA 510(k) clearance on 2005-08-25. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K052114.
When did BARD CONFORMEXX BILIARY STENT WITH THE PERFORMAXX GRIP receive FDA 510(k) clearance?
BARD CONFORMEXX BILIARY STENT WITH THE PERFORMAXX GRIP received FDA 510(k) clearance on 2005-08-25, under 510(k) number K052114.
Who is the listed applicant for BARD CONFORMEXX BILIARY STENT WITH THE PERFORMAXX GRIP?
The FDA 510(k) record lists Bard Peripheral Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARD CONFORMEXX BILIARY STENT WITH THE PERFORMAXX GRIP?
The FDA product code for BARD CONFORMEXX BILIARY STENT WITH THE PERFORMAXX GRIP 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 Bard Peripheral Vascular, 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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