CENTRAL VENOUS CATHETER
K-Number: K003839 · 2001-08-01
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Device Summary
Frequently Asked Questions
What is the CENTRAL VENOUS CATHETER?
CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 2001-08-01. The listed applicant is Boston Scientific Corp. The 510(k) number is K003839.
When did CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?
CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 2001-08-01, under 510(k) number K003839.
Who is the listed applicant for CENTRAL VENOUS CATHETER?
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTRAL VENOUS CATHETER?
The FDA product code for CENTRAL VENOUS CATHETER is LJS.
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 Boston Scientific 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: LJS)
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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