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FDA 510(k)

Sonopet iQ Ultrasonic Aspirator System

K-Number: K213824 · 2022-02-03

ApplicantStryker Corporation
Decision Date2022-02-03
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

Sonopet iQ Ultrasonic Aspirator System is a medical device manufactured by Stryker Corporation. It received FDA 510(k) clearance on 2022-02-03 under approval number K213824. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sonopet iQ Ultrasonic Aspirator System?

Sonopet iQ Ultrasonic Aspirator System is a medical device that received FDA 510(k) clearance on 2022-02-03. It is manufactured by Stryker Corporation. The 510(k) number is K213824.

When was Sonopet iQ Ultrasonic Aspirator System approved by the FDA?

Sonopet iQ Ultrasonic Aspirator System received FDA 510(k) clearance on 2022-02-03, under approval number K213824.

What company makes Sonopet iQ Ultrasonic Aspirator System?

Sonopet iQ Ultrasonic Aspirator System is manufactured by Stryker Corporation.

What is the FDA product code for Sonopet iQ Ultrasonic Aspirator System?

The FDA product code for Sonopet iQ Ultrasonic Aspirator System 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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