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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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