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FDA 510(k)

SOURCELINK

K-Number: K041576 · 2004-07-02

ApplicantC.R. Bard, Inc.
Decision Date2004-07-02
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOURCELINK is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2004-07-02 under 510(k) number K041576. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOURCELINK?

SOURCELINK is a medical device that received FDA 510(k) clearance on 2004-07-02. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K041576.

When did SOURCELINK receive FDA 510(k) clearance?

SOURCELINK received FDA 510(k) clearance on 2004-07-02, under 510(k) number K041576.

Who is the listed applicant for SOURCELINK?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOURCELINK?

The FDA product code for SOURCELINK is KXK.

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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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