Cleared Traditional

Stone Extraction Baskets

K230598 · Jiangsu Vedkang Medical Science and Technology Co., Ltd. · Gastroenterology & Urology
Sep 2023
Decision
193d
Days
Class 2
Risk

About This 510(k) Submission

K230598 is an FDA 510(k) clearance for the Stone Extraction Baskets, a Dislodger, Stone, Biliary (Class II — Special Controls, product code LQR), submitted by Jiangsu Vedkang Medical Science and Technology Co., Ltd. (Changzhou, CN). The FDA issued a Cleared decision on September 12, 2023, 193 days after receiving the submission on March 3, 2023. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5010.

Submission Details

510(k) Number K230598 FDA.gov
FDA Decision Cleared SESE
Date Received March 03, 2023
Decision Date September 12, 2023
Days to Decision 193 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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