FDA 510(k), K190070, Sonopet iQ Ultrasonic Aspirator System

FDA 510(k), K190070, Sonopet iQ Ultrasonic Aspirator System

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510(K) Number: K190070
Device Name: Sonopet iQ Ultrasonic Aspirator System
Manufacturer: Stryker Corporation
Device Classification Name: instrument, ultrasonic surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 01/15/2019
Decision Date: 04/11/2019
Regulation Medical Specialty:

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