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FDA 510(k)

Sonicision Cordless Ultrasonic Dissector

K-Number: K200427 · 2020-07-10

ApplicantCovidien, LLC
Decision Date2020-07-10
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

Sonicision Cordless Ultrasonic Dissector is a medical device manufactured by Covidien, LLC. It received FDA 510(k) clearance on 2020-07-10 under approval number K200427. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sonicision Cordless Ultrasonic Dissector?

Sonicision Cordless Ultrasonic Dissector is a medical device that received FDA 510(k) clearance on 2020-07-10. It is manufactured by Covidien, LLC. The 510(k) number is K200427.

When was Sonicision Cordless Ultrasonic Dissector approved by the FDA?

Sonicision Cordless Ultrasonic Dissector received FDA 510(k) clearance on 2020-07-10, under approval number K200427.

What company makes Sonicision Cordless Ultrasonic Dissector?

Sonicision Cordless Ultrasonic Dissector is manufactured by Covidien, LLC.

What is the FDA product code for Sonicision Cordless Ultrasonic Dissector?

The FDA product code for Sonicision Cordless Ultrasonic Dissector is LFL.

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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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