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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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