Avalon Laboratories, LLC - FDA 510(k) Cleared Devices
Recent clearances: AVALON ELITE VASCULAR ACCESS KIT, AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER, 13FR, 16FR, 19FR, 20FR, 23FR, 27FR, 31FR, AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, 24FR, 26FR, 28FR
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Avalon Laboratories, LLC Cardiovascular ✕
3 devices
Cleared
Nov 18, 2008
AVALON ELITE VASCULAR ACCESS KIT
Cardiovascular
133d
Cleared
Oct 06, 2008
AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER, 13FR, 16FR, 19FR, 20FR, 23FR,...
Cardiovascular
101d
Cleared
Oct 03, 2008
AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, 24FR, 26FR, 28FR
Cardiovascular
88d