Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare

K-Number: K220790 · 2022-06-27

Decision Date2022-06-27
Product CodeFDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare is a medical device manufactured by Yangzhou Fartley Medical Instrument Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-06-27 under approval number K220790. 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 Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare?

Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare is a medical device that received FDA 510(k) clearance on 2022-06-27. It is manufactured by Yangzhou Fartley Medical Instrument Technology Co., Ltd.. The 510(k) number is K220790.

When was Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare approved by the FDA?

Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare received FDA 510(k) clearance on 2022-06-27, under approval number K220790.

What company makes Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare?

Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare is manufactured by Yangzhou Fartley Medical Instrument Technology Co., Ltd..

What is the FDA product code for Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare?

The FDA product code for Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare is FDI.

Other Devices by Yangzhou Fartley Medical Instrument Technology Co., Ltd.

View all 7 devices →

Related Devices (Code: FDI)

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.