EDWARDS INTRODUCER SHEATH
K-Number: K031087 · 2003-04-24
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Device Summary
Frequently Asked Questions
What is the EDWARDS INTRODUCER SHEATH?
EDWARDS INTRODUCER SHEATH is a medical device that received FDA 510(k) clearance on 2003-04-24. The listed applicant is Edwards Lifesciences, LLC. The 510(k) number is K031087.
When did EDWARDS INTRODUCER SHEATH receive FDA 510(k) clearance?
EDWARDS INTRODUCER SHEATH received FDA 510(k) clearance on 2003-04-24, under 510(k) number K031087.
Who is the listed applicant for EDWARDS INTRODUCER SHEATH?
The FDA 510(k) record lists Edwards Lifesciences, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EDWARDS INTRODUCER SHEATH?
The FDA product code for EDWARDS INTRODUCER SHEATH is DYB.
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 Edwards Lifesciences, LLC 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: DYB)
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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