Avalon Laboratories, LLC is one of 24544 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Avalon Laboratories, LLC has 3 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 3 cleared submissions from 2008 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Avalon Laboratories, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avalon Laboratories, LLC
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