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FDA 510(k)

Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device

K-Number: K212301 · 2021-11-15

ApplicantCovidien, LLC
Decision Date2021-11-15
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device is a medical device manufactured by Covidien, LLC. It received FDA 510(k) clearance on 2021-11-15 under approval number K212301. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device?

Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device is a medical device that received FDA 510(k) clearance on 2021-11-15. It is manufactured by Covidien, LLC. The 510(k) number is K212301.

When was Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device approved by the FDA?

Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device received FDA 510(k) clearance on 2021-11-15, under approval number K212301.

What company makes Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device?

Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device is manufactured by Covidien, LLC.

What is the FDA product code for Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device?

The FDA product code for Sonicision 7 Curved Jaw Cordless Ultrasonic Dissection Device is LFL.

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Related Devices (Code: 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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