CUSA Clarity Ultrasonic Surgical Aspirator System
K-Number: K190180 · 2019-04-01
Device Summary
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 2019-04-01. It is manufactured by Integra LifeSciences Corporation. The 510(k) number is K190180.
When was CUSA Clarity Ultrasonic Surgical Aspirator System approved by the FDA?
CUSA Clarity Ultrasonic Surgical Aspirator System received FDA 510(k) clearance on 2019-04-01, under approval number K190180.
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.
Related Clinical Trials
Related PubMed Literature
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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.