Extraction Basket— 510(k) K243471

Name: FDA 510(k) clearance K243471
Creator: U.S. Food and Drug Administration
Published: 2024-12-16

Substantially Equivalent

Micro-Tech (Nanjing) Co., Ltd.

FDA 510(k) clearance K243471 for Extraction Basket, Substantially Equivalent on 2024-12-16. Applicant: Micro-Tech (Nanjing) Co., Ltd.. Device class: 2.

Clearance details

Applicant: Micro-Tech (Nanjing) Co., Ltd.
Product code: Product code LQR
Device class: Class 2
Regulation: 21 CFR 876.5010
Advisory panel: Gastroenterology, Urology
Date received: 2024-11-08
Decision date: 2024-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nanjing, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code LQR

view all

K253056 — Disposable Stone Extraction Basket2026-04-03
K243807 — Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P2025-03-18
K240192 — Single-use Extraction Baskets2024-10-15
K230598 — Stone Extraction Baskets2023-09-12
K203322 — SpyGlass Discover Retrieval Basket2021-05-26

More clearances from Micro-Tech (Nanjing) Co., Ltd.

view all

K261616 — Single-Use EBUS Balloon2026-10-15
K252492 — Visualized Access and Delivery Catheter; PB Digital Controller2026-04-24
K251692 — Advanced Tissue Resection Device2026-02-21
K250229 — Dual Action Tissue Closure Device2025-09-08
K243388 — Disposable Distal Cap2025-06-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.