FDA 510(k), K131973, UNEXEF-38G ULTRASOUND SYSTEM

FDA 510(k), K131973, UNEXEF-38G ULTRASOUND SYSTEM

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510(K) Number: K131973
Device Name: UNEXEF-38G ULTRASOUND SYSTEM
Manufacturer: TOYOTA TSUSHO CORPORATION
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 06/28/2013
Decision Date: 11/18/2014
Regulation Medical Specialty: Radiology
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