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

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K061936 KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311LJS2006-08-09 View
510(k) K030209 MAHURKAR OPLUS CATHETER, MODEL 13.5 FRMPB2003-05-13 View
510(k) K020089 MAHURKAR TRIPLE LUMEN CATHETER, 12 FRNIE2002-04-10 View
510(k) K011283 MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGENGT2001-10-15 View
510(k) K011941 EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088FRO2001-08-22 View
510(k) K002902 TANDEM-CATH 10 FR. CATHETER SYSTEM, MODEL MULTIPLE CODE NUMBERSMSD2001-04-09 View
510(k) K002901 KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETERMSD2001-03-28 View
510(k) K003313 FILAC FAS TEMP ELECTRONIC THERMOMETERFLL2001-01-11 View
↑