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FDA 510(k)

WILSON-COOK ENDOSCOPIC CLIPPING DEVICE

K-Number: K023903 · 2003-02-20

ApplicantWilson-Cook Medical, Inc.
Decision Date2003-02-20
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILSON-COOK ENDOSCOPIC CLIPPING DEVICE 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 2003-02-20 under 510(k) number K023903. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON-COOK ENDOSCOPIC CLIPPING DEVICE?

WILSON-COOK ENDOSCOPIC CLIPPING DEVICE is a medical device that received FDA 510(k) clearance on 2003-02-20. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K023903.

When did WILSON-COOK ENDOSCOPIC CLIPPING DEVICE receive FDA 510(k) clearance?

WILSON-COOK ENDOSCOPIC CLIPPING DEVICE received FDA 510(k) clearance on 2003-02-20, under 510(k) number K023903.

Who is the listed applicant for WILSON-COOK ENDOSCOPIC CLIPPING DEVICE?

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 ENDOSCOPIC CLIPPING DEVICE?

The FDA product code for WILSON-COOK ENDOSCOPIC CLIPPING DEVICE is PKL.

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Related Devices (Code: PKL)

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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