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


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