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 a medical device manufactured by Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2024-12-16 under approval 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. It is manufactured by Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K243471.
When was Extraction Basket approved by the FDA?
Extraction Basket received FDA 510(k) clearance on 2024-12-16, under approval number K243471.
What company makes Extraction Basket?
Extraction Basket is manufactured by Micro-Tech (Nanjing) Co., Ltd..
What is the FDA product code for Extraction Basket?
The FDA product code for Extraction Basket is LQR.
Other Devices by Micro-Tech (Nanjing) Co., Ltd.
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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.