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.

The Kendall Company Div. of Tyco Healthcare Group

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K024010 DOVER SILVER HYDROGEL COATED SILICONE FOLEY CATHETEREZL2003-06-11 View
510(k) K831081 EZEE FILTER/SEPARATORJKA1983-05-16 View
510(k) K831082 CONNECTING TUBINGBYX1983-05-09 View
510(k) K831079 LIQUIPETTEGJG1983-04-28 View
↑