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FDA 510(k)

CrossCath Support Catheter

K-Number: K161801 · 2016-07-29

ApplicantCook Incorporated
Decision Date2016-07-29
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CrossCath Support Catheter is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2016-07-29 under approval number K161801. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CrossCath Support Catheter?

CrossCath Support Catheter is a medical device that received FDA 510(k) clearance on 2016-07-29. It is manufactured by Cook Incorporated. The 510(k) number is K161801.

When was CrossCath Support Catheter approved by the FDA?

CrossCath Support Catheter received FDA 510(k) clearance on 2016-07-29, under approval number K161801.

What company makes CrossCath Support Catheter?

CrossCath Support Catheter is manufactured by Cook Incorporated.

What is the FDA product code for CrossCath Support Catheter?

The FDA product code for CrossCath Support Catheter is KRA.

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Other Devices by Cook Incorporated

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Related Devices (Code: KRA)

K161962VAMP Venous/Arterial Blood Management Protection SystemEdwards Lifesciences, LLC K160884CXI Support CatheterCook Incorporated K161921SwiftNINJA MicrocatheterMerit Medical Systems, Inc. K161402Bullfrog Micro-Infusion DeviceMercator Medsystems, Inc. K153501Bullfrog Micro-Infusion DeviceMercator Medsystems, Inc. K152625MMS Guide CatheterMicro Medical Solutions, Inc.

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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