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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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