FDA 510(k) Applications Submitted by STEPHEN M ENOS

FDA 510(k) Number Submission Date Device Name Applicant
K960159 01/11/1996 CORDIS STRAIGHT OR FINNED VENTR CATH (W/RADIO DOTS) CORDIS CORP.
K021593 05/15/2002 MODIFICATION TO ENVOY AND VISTA BRITE TIP CORDIS CORP.
K963839 09/24/1996 CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500 CORDIS CORP.
K955265 11/14/1995 CORDIS SHARP-ENDED STYLET; BLUNT-ENDED STYLET; CYST PUNCTURE CATHETER CORDIS CORP.
K955832 12/26/1995 CORDIS VENTRICULAR ANTECHAMBER (VA) CORDIS CORP.


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