Accutome Ultrasound, Inc. is one of 22877 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accutome Ultrasound, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ACCUPEN, B-SCAN PLUS, ACCUPACH V
3
Total
3
Cleared
0
Denied
Accutome Ultrasound, Inc. has 3 FDA 510(k) cleared medical devices. Based in Malvern, US.
Historical record: 3 cleared submissions from 2004 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Accutome Ultrasound, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Accutome Ultrasound, Inc.
3 devices