Medical Device Manufacturer · US , Mansfield , MA

Tyco Healthcare/Kendall - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2004

Total

Cleared

Denied

Tyco Healthcare/Kendall has 4 FDA 510(k) cleared medical devices. Based in Mansfield, US.

Historical record: 4 cleared submissions from 2004 to 2006. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Tyco Healthcare/Kendall Filter by specialty or product code using the sidebar.

Tyco Healthcare/Kendall is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tyco Healthcare/Kendall

4 devices

1-4 of 4