Cleared Traditional

Disposable Stone Extraction basket

K201509 · Hangzhou AGS MedTech Co., Ltd. · Gastroenterology & Urology
Dec 2020
Decision
194d
Days
Class 2
Risk

About This 510(k) Submission

K201509 is an FDA 510(k) clearance for the Disposable Stone Extraction basket, a Dislodger, Stone, Biliary (Class II — Special Controls, product code LQR), submitted by Hangzhou AGS MedTech Co., Ltd. (Hangzhou, CN). The FDA issued a Cleared decision on December 16, 2020, 194 days after receiving the submission on June 5, 2020. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5010.

Submission Details

510(k) Number K201509 FDA.gov
FDA Decision Cleared SESE
Date Received June 05, 2020
Decision Date December 16, 2020
Days to Decision 194 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code LQR — Dislodger, Stone, Biliary
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.5010

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