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. The listed applicant is Yangzhou Fartley Medical Instrument Technology Co., Ltd.. The 510(k) number is K220790.
When did Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare receive FDA 510(k) clearance?
Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare received FDA 510(k) clearance on 2022-06-27, under 510(k) number K220790.
Who is the listed applicant for Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare?
The FDA 510(k) record lists Yangzhou Fartley Medical Instrument Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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 records listing Yangzhou Fartley Medical Instrument Technology Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FDI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.