Cordis Webster, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL #'S 301-803A, 301-803P, 301-803M, 301-813S, CORDIS WEBSTER REF-STAR EXTERNAL REFERENCE PATCH, MODEL # D-1210, CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Webster, Inc. Cardiovascular ✕
10 devices
Cleared
Nov 26, 1999
CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085
Cardiovascular
85d
Cleared
Oct 04, 1999
CORDIS WEBSTER DIAGNOSTIC DEFLECTABLE TIP CATHETER, MODEL D-1078
Cardiovascular
154d
Cleared
Aug 28, 1998
CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL...
Cardiovascular
22d
Cleared
Aug 10, 1998
CORDIS WEBSTER REF-STAR EXTERNAL REFERENCE PATCH, MODEL # D-1210
Cardiovascular
28d
Cleared
May 28, 1998
CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01,...
Cardiovascular
73d
Cleared
Oct 28, 1997
CORDIS WEBSTER BRAIDED GUIDING SHEATH EXCHANGE SYSTEM
Cardiovascular
278d
Cleared
Sep 18, 1996
CORDIS WEBSTER T20 DIAGNOSTIC DEFLECTABLE TIP CATHETER
Cardiovascular
408d
Cleared
Mar 25, 1996
CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER
Cardiovascular
90d
Cleared
Dec 21, 1995
CORDIS WESTER STAR CATHETER
Cardiovascular
93d
Cleared
Nov 22, 1995
CORDIS WEBSTER A20 DIAGNOSTIC DEFLECTABLE TIP CATHETER
Cardiovascular
100d