Tyco Healthcare Group is one of 16058 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tyco Healthcare Group - FDA 510(k) Cleared Devices
Recent clearances: POLYSORB* SYNTHETIC ABSORBABLE SUTURE WITH MODIFIED PACKAGING, PALINDROME EMERALD 14.5 FR CHRONIC HEMODIALYSIS CATHETER WITH HEPARIN COATING
2
Total
2
Cleared
0
Denied
Tyco Healthcare Group has 2 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Tyco Healthcare Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tyco Healthcare Group
2 devices