Covidien Lp, Formerly Registered AS Kendall is one of 5230 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...
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.
Covidien Lp, Formerly Registered AS Kendall — FDA 510(k) Products and Clearance History
3 devices
Cleared
Apr 17, 2013
MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.
General Hospital
30d
Cleared
May 11, 2012
DOBBHOFF DUAL PORT FEEDING TUBE
Gastroenterology & Urology
255d
Cleared
Oct 30, 2009
PALINDROME P HEMODIALYSIS CATHETER
Gastroenterology & Urology
100d