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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 the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2018-03-22 under 510(k) 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. The listed applicant is Cook Incorporated. The 510(k) number is K173105.

When did Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter receive FDA 510(k) clearance?

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

Who is the listed applicant for Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter?

The FDA 510(k) record lists Cook Incorporated as the applicant. This does not by itself establish the device manufacturer.

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.

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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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