Ecton, Inc. is one of 7892 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ecton, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ECTON LYNX ULTRASOUND SYSTEM
2
Total
2
Cleared
0
Denied
Ecton, Inc. has 2 FDA 510(k) cleared medical devices. Based in Ambler, US.
Historical record: 2 cleared submissions from 1998 to 1999. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ecton, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Ecton, Inc.
2 devices