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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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