Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare

FDA 510(k) K220790 · Yangzhou Fartley Medical Instrument Technology Co., Ltd.

Substantially Equivalent

510(k) numberK220790

Submission

Device name
Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare
Applicant
Yangzhou Fartley Medical Instrument Technology Co., Ltd.
Yangzhou, CN
Received
March 17, 2022
Decision date
June 27, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FDI – Snare, Flexible
Device class
Class II (moderate risk)
Regulation
21 CFR 876.4300
Specialty
Gastroenterology, Urology

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Questions and answers

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

Disposable Polypectomy Snare, Disposable Polypectomy Hybrid Snare (K220790) received a 510(k) decision of Substantially Equivalent on June 27, 2022, 102 days after the submission was received.

What is the product code of K220790?

The FDA product code is FDI – Snare, Flexible, a Class II (moderate risk) device regulated under 21 CFR 876.4300.