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FDA 510(k)

AcuSnare Polypectomy Snare

K-Number: K173673 · 2018-08-24

ApplicantWilson-Cook Medical, Inc.
Decision Date2018-08-24
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AcuSnare Polypectomy Snare is a medical device manufactured by Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2018-08-24 under approval number K173673. 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?

AcuSnare Polypectomy Snare is a medical device that received FDA 510(k) clearance on 2018-08-24. It is manufactured by Wilson-Cook Medical, Inc.. The 510(k) number is K173673.

When was AcuSnare Polypectomy Snare approved by the FDA?

AcuSnare Polypectomy Snare received FDA 510(k) clearance on 2018-08-24, under approval number K173673.

What company makes AcuSnare Polypectomy Snare?

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

What is the FDA product code for AcuSnare Polypectomy Snare?

The FDA product code for AcuSnare Polypectomy Snare is FDI.

Other Devices by Wilson-Cook Medical, Inc.

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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. K172729Polypectomy SnareHangzhou AGS MedTech Co., Ltd. K172758Rotatable Snares, Non-Rotatable SnaresZhejiang Chuangxiang Medical Technology Co., Ltd. K190512SmartBand EMR Kit, SmartBand EMR Pack, SmartSnareIntelligent Endoscopy

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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