FDA 510(k) Applications Submitted by AVALON LABORATORIES, LLC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K081820 |
06/27/2008 |
AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER, 13FR, 16FR, 19FR, 20FR, 23FR, 27FR, 31FR |
AVALON LABORATORIES, LLC |
K081933 |
07/07/2008 |
AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, 24FR, 26FR, 28FR |
AVALON LABORATORIES, LLC |
K081940 |
07/08/2008 |
AVALON ELITE VASCULAR ACCESS KIT |
AVALON LABORATORIES, LLC |
|
|