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Covidien Lp, Formerly Registered AS Kendall

3 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR. (K130725)Covidien Lp, Formerly Registered AS Kendall2013-04-17
DOBBHOFF DUAL PORT FEEDING TUBE (K112511)Covidien Lp, Formerly Registered AS Kendall2012-05-11
PALINDROME P HEMODIALYSIS CATHETER (K092205)Covidien Lp, Formerly Registered AS Kendall2009-10-30

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Every clearance here is in the API, with alerts when new ones post.