DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM
K-Number: K014007 · 2002-01-07
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Device Summary
Frequently Asked Questions
What is the DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM?
DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM is a medical device that received FDA 510(k) clearance on 2002-01-07. The listed applicant is Guidant Corp.. The 510(k) number is K014007.
When did DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM receive FDA 510(k) clearance?
DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM received FDA 510(k) clearance on 2002-01-07, under 510(k) number K014007.
Who is the listed applicant for DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM?
The FDA 510(k) record lists Guidant Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM?
The FDA product code for DYNALINK .018 BILLARY SELF-EXPANDING STENT 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 Guidant 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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