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FDA 510(k)

Single-use Extraction Baskets

K-Number: K240192 · 2024-10-15

ApplicantScivita Medical Technology Co., Ltd.
Decision Date2024-10-15
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Single-use Extraction Baskets is a medical device manufactured by Scivita Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-10-15 under approval number K240192. 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 Single-use Extraction Baskets?

Single-use Extraction Baskets is a medical device that received FDA 510(k) clearance on 2024-10-15. It is manufactured by Scivita Medical Technology Co., Ltd.. The 510(k) number is K240192.

When was Single-use Extraction Baskets approved by the FDA?

Single-use Extraction Baskets received FDA 510(k) clearance on 2024-10-15, under approval number K240192.

What company makes Single-use Extraction Baskets?

Single-use Extraction Baskets is manufactured by Scivita Medical Technology Co., Ltd..

What is the FDA product code for Single-use Extraction Baskets?

The FDA product code for Single-use Extraction Baskets is LQR.

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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.

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