Cordis Webster, Inc.

10FDA 510(k) medical device clearances.

Top product codes for Cordis Webster, Inc.

DRF — Cardiovascular8 devices
DYB — Cardiovascular2 devices

Recent clearances by Cordis Webster, Inc.

K992965 — CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085Code DRF·1999-11-26
K991531 — CORDIS WEBSTER DIAGNOSTIC DEFLECTABLE TIP CATHETER, MODEL D-1078Code DRF·1999-10-04
K982740 — CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL #'S 301-803A, 301-803P, 301-803M, 301-813SCode DYB·1998-08-28
K982415 — CORDIS WEBSTER REF-STAR EXTERNAL REFERENCE PATCH, MODEL # D-1210Code DRF·1998-08-10
K980961 — CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.Code DRF·1998-05-28
K970264 — CORDIS WEBSTER BRAIDED GUIDING SHEATH EXCHANGE SYSTEMCode DYB·1997-10-28
K953663 — CORDIS WEBSTER T20 DIAGNOSTIC DEFLECTABLE TIP CATHETERCode DRF·1996-09-18
K955817 — CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETERCode DRF·1996-03-25
K954390 — CORDIS WESTER STAR CATHETERCode DRF·1995-12-21
K953768 — CORDIS WEBSTER A20 DIAGNOSTIC DEFLECTABLE TIP CATHETERCode DRF·1995-11-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.