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FDA 510(k)

WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH

K-Number: K040324 · 2004-05-20

ApplicantWilson-Cook Medical, Inc.
Decision Date2004-05-20
Product CodeFDX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2004-05-20 under 510(k) number K040324. The device is classified under product code FDX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH?

WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH is a medical device that received FDA 510(k) clearance on 2004-05-20. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K040324.

When did WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH receive FDA 510(k) clearance?

WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH received FDA 510(k) clearance on 2004-05-20, under 510(k) number K040324.

Who is the listed applicant for WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH?

The FDA 510(k) record lists Wilson-Cook Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH?

The FDA product code for WILSON-COOK DOUBLE LUMEN BILIARY CYTOLOGY BRUSH is FDX.

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Related Devices (Code: FDX)

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.

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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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