Kendall
Kendall holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2009.
Top product codes for Kendall
Recent clearances by Kendall
- K092797 — ACUTE AND CHRONIC CATHETER REPAIR KIT
- K062671 — 14.5 FR CHRONIC HEMODIALYSIS CATHETER WITH HEPARIN COATING AND SILVER IMPREGNATED SLEEVE (PALINDROME SAPPHIRE)
- K060972 — KEDALL 14.5 FR CHRONIC HEMODIALYSIS CATHETER W/SILVER IMPREGNATED SLEEVE (PALINDROME RUBY)
- K053410 — GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTOR
- K051584 — 14.5 FR CHRONIC HEMODIALYSIS CATHETER WITH INSERTION STYLETS ACCESSORY
- K043272 — PALLINDROME 14.5FR CHRONIC HEMODIALYSIS CATHETER WITH SLOTTED SYMMETRICAL TIP
- K042461 — KENDALL ARGYLE 2 FR DOUBLE LUMEN NEONATAL/PEDIATRIC PICC, MODEL 43304
- K042572 — KENDALL CO2NFIRM NOW CO2 DETECTOR
- K041914 — PALLINDROME 14.5FR CHRONIC HEMODIALYSIS CATHETER
- K041006 — TANDEM-CATH HEMODIALYSIS CATHETER, MODEL 10 FR
- K040388 — NEXT GENERATION SALEM SUMP
- K033676 — PALINDROME 14.5 FR CHRONIC HEMODIALYSIS CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.