Activatek, Inc. is one of 5644 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Activatek, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Activatek, Inc. has 3 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 3 cleared submissions from 2006 to 2014. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Activatek, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Activatek, Inc.
3 devices