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FDA 510(k)

Extraction Basket

K-Number: K243471 · 2024-12-16

ApplicantMicro-Tech (Nanjing) Co., Ltd.
Decision Date2024-12-16
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Extraction Basket is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2024-12-16 under 510(k) number K243471. The device is classified under product code LQR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Extraction Basket?

Extraction Basket is a medical device that received FDA 510(k) clearance on 2024-12-16. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K243471.

When did Extraction Basket receive FDA 510(k) clearance?

Extraction Basket received FDA 510(k) clearance on 2024-12-16, under 510(k) number K243471.

Who is the listed applicant for Extraction Basket?

The FDA 510(k) record lists Micro-Tech (Nanjing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Extraction Basket?

The FDA product code for Extraction Basket is LQR.

Other records listing Micro-Tech (Nanjing) Co., Ltd. as applicant

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Related Devices (Code: LQR)

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.

K253056Disposable Stone Extraction BasketZhejiang Soudon Medical Technology Co., Ltd.K243807Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432POlympus Medical Systems Corp.K240192Single-use Extraction BasketsScivita Medical Technology Co., Ltd.K230598Stone Extraction BasketsJiangsu Vedkang Medical Science and Technology Co., Ltd.K203322SpyGlass Discover Retrieval BasketBoston Scientific CorporationK201509Disposable Stone Extraction basketHangzhou AGS MedTech Co., Ltd.

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.

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