Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Covidien Lp, Formerly Registered AS Kendall

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130725 MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.FOS2013-04-17 View
510(k) K112511 DOBBHOFF DUAL PORT FEEDING TUBEKNT2012-05-11 View
510(k) K092205 PALINDROME P HEMODIALYSIS CATHETERMSD2009-10-30 View
↑