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Covidien Lp, Formerly Registered AS Kendall

FDA Regulatory Profile

Covidien Lp, Formerly Registered AS Kendall appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 17, 2013.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.April 17, 2013
K112511DOBBHOFF DUAL PORT FEEDING TUBEMay 11, 2012
K092205PALINDROME P HEMODIALYSIS CATHETEROctober 30, 2009

FDA data resources