Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare
K-Number: K220790 · 2022-06-27
Device Summary
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.
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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.