FDA 510(k) Applications Submitted by WARTNER MEDICAL PRODUCTS

FDA 510(k) Number Submission Date Device Name Applicant
K002714 08/31/2000 WARTNER WART REMOVAL SYSTEM WARTNER MEDICAL PRODUCTS
K030838 03/17/2003 WARTNER PRO WARTNER MEDICAL PRODUCTS
K011708 06/04/2001 MODIFICATION TO WARTNER WART REMOVAL SYSTEM WARTNER MEDICAL PRODUCTS


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