FDA 510(k)

COOK IRELAND ECHOBRUSH

K-Number: K052279 · 2005-10-11

Decision Date2005-10-11

Product CodeFDX

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

COOK IRELAND ECHOBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ireland, Ltd.. It received FDA 510(k) clearance on 2005-10-11 under 510(k) number K052279. The device is classified under product code FDX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOK IRELAND ECHOBRUSH?

COOK IRELAND ECHOBRUSH is a medical device that received FDA 510(k) clearance on 2005-10-11. The listed applicant is Cook Ireland, Ltd.. The 510(k) number is K052279.

When did COOK IRELAND ECHOBRUSH receive FDA 510(k) clearance?

COOK IRELAND ECHOBRUSH received FDA 510(k) clearance on 2005-10-11, under 510(k) number K052279.

Who is the listed applicant for COOK IRELAND ECHOBRUSH?

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

What is the FDA product code for COOK IRELAND ECHOBRUSH?

The FDA product code for COOK IRELAND ECHOBRUSH is FDX.

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Related Devices (Code: FDX)

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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.