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FDA 510(k)

Ultrasonic Surgical System

K-Number: K233036 · 2024-06-18

Decision Date2024-06-18
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

Ultrasonic Surgical System is a medical device manufactured by Hunan Handlike Minimally Invasive Surgery Co., Ltd.. It received FDA 510(k) clearance on 2024-06-18 under approval number K233036. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ultrasonic Surgical System?

Ultrasonic Surgical System is a medical device that received FDA 510(k) clearance on 2024-06-18. It is manufactured by Hunan Handlike Minimally Invasive Surgery Co., Ltd.. The 510(k) number is K233036.

When was Ultrasonic Surgical System approved by the FDA?

Ultrasonic Surgical System received FDA 510(k) clearance on 2024-06-18, under approval number K233036.

What company makes Ultrasonic Surgical System?

Ultrasonic Surgical System is manufactured by Hunan Handlike Minimally Invasive Surgery Co., Ltd..

What is the FDA product code for Ultrasonic Surgical System?

The FDA product code for Ultrasonic Surgical System is LFL.

Related Clinical Trials

Related PubMed Literature

Other Devices by Hunan Handlike Minimally Invasive Surgery Co., Ltd.

Related Devices (Code: LFL)

Official Source

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