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FDA 510(k)

Rotatable Snares, Non-Rotatable Snares

K-Number: K172758 · 2018-03-07

ApplicantZhejiang Chuangxiang Medical Technology Co., Ltd.
Decision Date2018-03-07
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Rotatable Snares, Non-Rotatable Snares is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Chuangxiang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-03-07 under 510(k) number K172758. 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 Rotatable Snares, Non-Rotatable Snares?

Rotatable Snares, Non-Rotatable Snares is a medical device that received FDA 510(k) clearance on 2018-03-07. The listed applicant is Zhejiang Chuangxiang Medical Technology Co., Ltd.. The 510(k) number is K172758.

When did Rotatable Snares, Non-Rotatable Snares receive FDA 510(k) clearance?

Rotatable Snares, Non-Rotatable Snares received FDA 510(k) clearance on 2018-03-07, under 510(k) number K172758.

Who is the listed applicant for Rotatable Snares, Non-Rotatable Snares?

The FDA 510(k) record lists Zhejiang Chuangxiang Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Rotatable Snares, Non-Rotatable Snares?

The FDA product code for Rotatable Snares, Non-Rotatable Snares 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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