COOK FIVE LUMEN CENTRAL VENOUS CATHETER
K-Number: K032274 · 2004-02-26
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Device Summary
Frequently Asked Questions
What is the COOK FIVE LUMEN CENTRAL VENOUS CATHETER?
COOK FIVE LUMEN CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 2004-02-26. The listed applicant is Cook, Inc.. The 510(k) number is K032274.
When did COOK FIVE LUMEN CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?
COOK FIVE LUMEN CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 2004-02-26, under 510(k) number K032274.
Who is the listed applicant for COOK FIVE LUMEN CENTRAL VENOUS CATHETER?
The FDA 510(k) record lists Cook, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COOK FIVE LUMEN CENTRAL VENOUS CATHETER?
The FDA product code for COOK FIVE LUMEN CENTRAL VENOUS CATHETER is FOZ.
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, 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: FOZ)
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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