Covidien Lp, Formerly Registered AS Kendall

Covidien Lp, Formerly Registered AS Kendall holds 3 FDA 510(k) medical device clearances, first cleared 2009, most recent 2013.

Top product codes for Covidien Lp, Formerly Registered AS Kendall

Recent clearances by Covidien Lp, Formerly Registered AS Kendall

K130725 — MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.Code FOS·2013-04-17
K112511 — DOBBHOFF DUAL PORT FEEDING TUBECode KNT·2012-05-11
K092205 — PALINDROME P HEMODIALYSIS CATHETERCode MSD·2009-10-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.