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FDA 510(k)

COOK IRELAND SONNET POLYPECTOMY SNARE

K-Number: K050294 · 2005-03-31

ApplicantCook Ireland, Ltd.
Decision Date2005-03-31
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COOK IRELAND SONNET POLYPECTOMY SNARE 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 2005-03-31 under 510(k) number K050294. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOK IRELAND SONNET POLYPECTOMY SNARE?

COOK IRELAND SONNET POLYPECTOMY SNARE is a medical device that received FDA 510(k) clearance on 2005-03-31. The listed applicant is Cook Ireland, Ltd.. The 510(k) number is K050294.

When did COOK IRELAND SONNET POLYPECTOMY SNARE receive FDA 510(k) clearance?

COOK IRELAND SONNET POLYPECTOMY SNARE received FDA 510(k) clearance on 2005-03-31, under 510(k) number K050294.

Who is the listed applicant for COOK IRELAND SONNET POLYPECTOMY SNARE?

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 SONNET POLYPECTOMY SNARE?

The FDA product code for COOK IRELAND SONNET POLYPECTOMY SNARE is FDI.

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Related Devices (Code: FDI)

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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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