Medical Device Manufacturer · US , Salt Lake City , UT

Activatek, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2006

Total

Cleared

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.

Activatek, Inc. is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Activatek, Inc. — FDA 510(k) Products and Clearance History

3 devices

1-3 of 3