MARATHON STENT WITH FUSION TECHNOLOGY
K-Number: K060624 · 2006-08-04
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Device Summary
Frequently Asked Questions
What is the MARATHON STENT WITH FUSION TECHNOLOGY?
MARATHON STENT WITH FUSION TECHNOLOGY is a medical device that received FDA 510(k) clearance on 2006-08-04. The listed applicant is Cook Ireland, Ltd.. The 510(k) number is K060624.
When did MARATHON STENT WITH FUSION TECHNOLOGY receive FDA 510(k) clearance?
MARATHON STENT WITH FUSION TECHNOLOGY received FDA 510(k) clearance on 2006-08-04, under 510(k) number K060624.
Who is the listed applicant for MARATHON STENT WITH FUSION TECHNOLOGY?
The FDA 510(k) record lists Cook Ireland, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MARATHON STENT WITH FUSION TECHNOLOGY?
The FDA product code for MARATHON STENT WITH FUSION TECHNOLOGY 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 Cook Ireland, Ltd. 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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