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FDA 510(k)

Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter

K-Number: K173105 · 2018-03-22

ApplicantCook Incorporated
Decision Date2018-03-22
Product CodeODC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2018-03-22 under approval number K173105. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter?

Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter is a medical device that received FDA 510(k) clearance on 2018-03-22. It is manufactured by Cook Incorporated. The 510(k) number is K173105.

When was Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter approved by the FDA?

Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter received FDA 510(k) clearance on 2018-03-22, under approval number K173105.

What company makes Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter?

Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter is manufactured by Cook Incorporated.

What is the FDA product code for Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter?

The FDA product code for Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter is ODC.

Related Clinical Trials

NCT07495137 The Improvement Effect of Real-time Artificial Intelligence Assisted Identification of Bleeding Points on Hemostasis Efficiency in Endoscopic Submucosal Dissection NOT_YET_RECRUITING

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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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