FDA 510(k) Applications Submitted by Mary Adams

FDA 510(k) Number Submission Date Device Name Applicant
K970264 01/23/1997 CORDIS WEBSTER BRAIDED GUIDING SHEATH EXCHANGE SYSTEM CORDIS WEBSTER, INC.
K980961 03/16/1998 CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04. CORDIS WEBSTER, INC.
K001139 04/10/2000 PREFACE GUIDING SHEATH, MODELS 2-603M, 2-703M, 2-803M, 2-903M, 2-1003M, 2-1103M BIOSENSE WEBSTER, INC.
K991531 05/03/1999 CORDIS WEBSTER DIAGNOSTIC DEFLECTABLE TIP CATHETER, MODEL D-1078 CORDIS WEBSTER, INC.
K231311 05/05/2023 CPS DirectÖ Universal slittable outer guide catheter (DS2C029) Abbott Medical
K982415 07/13/1998 CORDIS WEBSTER REF-STAR EXTERNAL REFERENCE PATCH, MODEL # D-1210 CORDIS WEBSTER, INC.
K982740 08/06/1998 CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL #'S 301-803A, 301-803P, 301-803M, 301-813S CORDIS WEBSTER, INC.
K953663 08/07/1995 CORDIS WEBSTER T20 DIAGNOSTIC DEFLECTABLE TIP CATHETER CORDIS WEBSTER, INC.
K162313 08/18/2016 NuVasive Next Generation NVM5 System NUVASIVE INCORPORATED
K992965 09/02/1999 CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085 CORDIS WEBSTER, INC.
K955817 12/26/1995 CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER CORDIS WEBSTER, INC.


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