FDA 510(k), K192107, Clarius Ultrasound Scanner

FDA 510(k), K192107, Clarius Ultrasound Scanner

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510(K) Number: K192107
Device Name: Clarius Ultrasound Scanner
Manufacturer: Clarius Mobile Health Corp.
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 08/05/2019
Decision Date: 08/29/2019
Regulation Medical Specialty: Radiology

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