FDA 510(k), K171301, Scanmate Flex

FDA 510(k), K171301, Scanmate Flex

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510(K) Number: K171301
Device Name: Scanmate Flex
Manufacturer: DGH Technology, Inc.
Device Classification Name: system, imaging, pulsed echo, ultrasonic
Regulation Number: 892.1560
Classification Product Code: IYO
Date Received: 05/03/2017
Decision Date: 07/31/2017
Regulation Medical Specialty: Radiology

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