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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 the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2018-08-24 under 510(k) 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. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K173673.

When did AcuSnare Polypectomy Snare receive FDA 510(k) clearance?

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

Who is the listed applicant for AcuSnare Polypectomy Snare?

The FDA 510(k) record lists Wilson-Cook Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AcuSnare Polypectomy Snare?

The FDA product code for AcuSnare Polypectomy Snare is 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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