FDA 510(k) Applications Submitted by MARLENE VALENTI

FDA 510(k) Number Submission Date Device Name Applicant
K955637 12/11/1995 ESSENCE GUIDEWIRE CORDIS NEUROVASCULAR, INC.
K962746 07/15/1996 CORDIS AVANTI TRANS-RADIAL CATHETER SHEATH INTRODUCER KIT CORDIS CORP.
K955728 12/18/1995 CORDIS BILIARY STENT CORDIS CORP.


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