FDA 510(k), K963807, TOMTEC ECHO-SCAN

FDA 510(k), K963807, TOMTEC ECHO-SCAN

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510(K) Number: K963807
Device Name: TOMTEC ECHO-SCAN
Manufacturer:
Device Classification Name: System, Imaging, Pulsed Echo, Ultrasonic
Regulation Number: 892.1560
Classification Product Code: IYO
Date Received: 09/23/1996
Decision Date: 12/18/1996
Regulation Medical Specialty: Radiology
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