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FDA 510(k)

CUSA Clarity Ultrasonic Surgical Aspirator System

K-Number: K200774 · 2020-06-23

Decision Date2020-06-23
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

CUSA Clarity Ultrasonic Surgical Aspirator System is a medical device manufactured by Integra LifeSciences Corporation. It received FDA 510(k) clearance on 2020-06-23 under approval number K200774. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSA Clarity Ultrasonic Surgical Aspirator System?

CUSA Clarity Ultrasonic Surgical Aspirator System is a medical device that received FDA 510(k) clearance on 2020-06-23. It is manufactured by Integra LifeSciences Corporation. The 510(k) number is K200774.

When was CUSA Clarity Ultrasonic Surgical Aspirator System approved by the FDA?

CUSA Clarity Ultrasonic Surgical Aspirator System received FDA 510(k) clearance on 2020-06-23, under approval number K200774.

What company makes CUSA Clarity Ultrasonic Surgical Aspirator System?

CUSA Clarity Ultrasonic Surgical Aspirator System is manufactured by Integra LifeSciences Corporation.

What is the FDA product code for CUSA Clarity Ultrasonic Surgical Aspirator System?

The FDA product code for CUSA Clarity Ultrasonic Surgical Aspirator System is LFL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.