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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