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FDA 510(k)

Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter

K-Number: K171810 · 2018-03-07

ApplicantCook Incorporated
Decision Date2018-03-07
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2018-03-07 under approval number K171810. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter?

Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter is a medical device that received FDA 510(k) clearance on 2018-03-07. It is manufactured by Cook Incorporated. The 510(k) number is K171810.

When was Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter approved by the FDA?

Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter received FDA 510(k) clearance on 2018-03-07, under approval number K171810.

What company makes Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter?

Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter is manufactured by Cook Incorporated.

What is the FDA product code for Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter?

The FDA product code for Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter is KOD.

Related Clinical Trials

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Related Devices (Code: KOD)

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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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