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FDA 510(k)

AcuSnare Polypectomy Snare - Duckbill

K-Number: K191048 · 2019-07-18

ApplicantWilson-Cook Medical, Inc.
Decision Date2019-07-18
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AcuSnare Polypectomy Snare - Duckbill is a medical device manufactured by Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2019-07-18 under approval number K191048. 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 AcuSnare Polypectomy Snare - Duckbill?

AcuSnare Polypectomy Snare - Duckbill is a medical device that received FDA 510(k) clearance on 2019-07-18. It is manufactured by Wilson-Cook Medical, Inc.. The 510(k) number is K191048.

When was AcuSnare Polypectomy Snare - Duckbill approved by the FDA?

AcuSnare Polypectomy Snare - Duckbill received FDA 510(k) clearance on 2019-07-18, under approval number K191048.

What company makes AcuSnare Polypectomy Snare - Duckbill?

AcuSnare Polypectomy Snare - Duckbill is manufactured by Wilson-Cook Medical, Inc..

What is the FDA product code for AcuSnare Polypectomy Snare - Duckbill?

The FDA product code for AcuSnare Polypectomy Snare - Duckbill is FDI.

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Related Devices (Code: FDI)

K160637Rotatable SnaresBoston Scientific Corporation K172734Single Use Electrosurgical Snare SD-400Olympus Medical Systems Corp. K182909Roth Net Retriever Product LineUnited States Endoscopy Group, Inc. K173673AcuSnare Polypectomy SnareWilson-Cook Medical, Inc. K172729Polypectomy SnareHangzhou AGS MedTech Co., Ltd. K172758Rotatable Snares, Non-Rotatable SnaresZhejiang Chuangxiang Medical Technology Co., Ltd.

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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