FDA 510(k) Applications Submitted by EUROMED A/S

FDA 510(k) Number Submission Date Device Name Applicant
K960393 01/29/1996 SURESKIN BORDER EUROMED A/S
K960394 01/29/1996 SURESKIN STANDARD EUROMED A/S
K960404 01/29/1996 SURESKIN THIN EUROMED A/S
K963039 08/05/1996 SURESKIN STANDARD, BORDER, AND THIN EUROMED A/S


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