Cordis Webster, Inc.
Cordis Webster, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 1999.
Top product codes for Cordis Webster, Inc.
Recent clearances by Cordis Webster, Inc.
- K992965 — CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085
- K991531 — CORDIS WEBSTER DIAGNOSTIC DEFLECTABLE TIP CATHETER, MODEL D-1078
- K982740 — CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL #'S 301-803A, 301-803P, 301-803M, 301-813S
- K982415 — CORDIS WEBSTER REF-STAR EXTERNAL REFERENCE PATCH, MODEL # D-1210
- K980961 — CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.
- K970264 — CORDIS WEBSTER BRAIDED GUIDING SHEATH EXCHANGE SYSTEM
- K953663 — CORDIS WEBSTER T20 DIAGNOSTIC DEFLECTABLE TIP CATHETER
- K955817 — CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER
- K954390 — CORDIS WESTER STAR CATHETER
- K953768 — CORDIS WEBSTER A20 DIAGNOSTIC DEFLECTABLE TIP CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.