FDA 510(k) Applications Submitted by LEE WIRTH

FDA 510(k) Number Submission Date Device Name Applicant
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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