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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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