The Kendall Company
The Kendall Company holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2006.
Top product codes for The Kendall Company
Recent clearances by The Kendall Company
- K061936 — KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311
- K030209 — MAHURKAR OPLUS CATHETER, MODEL 13.5 FR
- K020089 — MAHURKAR TRIPLE LUMEN CATHETER, 12 FR
- K011283 — MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE
- K011941 — EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088
- K002902 — TANDEM-CATH 10 FR. CATHETER SYSTEM, MODEL MULTIPLE CODE NUMBERS
- K002901 — KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER
- K003313 — FILAC FAS TEMP ELECTRONIC THERMOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.