FDA 510(k) Applications Submitted by COVIDIEN LP, FORMERLY REGISTERED AS KENDALL

FDA 510(k) Number Submission Date Device Name Applicant
K092205 07/22/2009 PALINDROME P HEMODIALYSIS CATHETER COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
K112511 08/30/2011 DOBBHOFF DUAL PORT FEEDING TUBE COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
K130725 03/18/2013 MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR. COVIDIEN LP, FORMERLY REGISTERED AS KENDALL


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