Covidien Lp, Formerly Registered AS Kendall is one of 15076 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Covidien Lp, Formerly Registered AS Kendall - FDA 510(k) Cleared Devi...
Recent clearances: MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR., DOBBHOFF DUAL PORT FEEDING TUBE, PALINDROME P HEMODIALYSIS CATHETER
3
Total
2
Cleared
0
Denied
Covidien Lp, Formerly Registered AS Kendall has 2 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 2 cleared submissions from 2009 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Covidien Lp, Formerly Registered AS Kendall Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Covidien Lp, Formerly Registered AS Kendall
3 devices