ClearanceBrief
Company ยท US

Cordis Webster, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1999. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DRFCatheter, Electrode Recording, Or Probe, Electrode Recording8
DYBIntroducer, Catheter2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 26, 1999K992965CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085
Cordis Webster, Inc.
DRF
Oct 4, 1999K991531CORDIS WEBSTER DIAGNOSTIC DEFLECTABLE TIP CATHETER, MODEL D-1078
Cordis Webster, Inc.
DRF
Aug 28, 1998K982740CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL #'S 301-803A, 301-803P, 301-803M, 301-813S
Cordis Webster, Inc.
DYB
Aug 10, 1998K982415CORDIS WEBSTER REF-STAR EXTERNAL REFERENCE PATCH, MODEL # D-1210
Cordis Webster, Inc.
DRF
May 28, 1998K980961CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.
Cordis Webster, Inc.
DRF
Oct 28, 1997K970264CORDIS WEBSTER BRAIDED GUIDING SHEATH EXCHANGE SYSTEM
Cordis Webster, Inc.
DYB
Sep 18, 1996K953663CORDIS WEBSTER T20 DIAGNOSTIC DEFLECTABLE TIP CATHETER
Cordis Webster, Inc.
DRF
Mar 25, 1996K955817CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER
Cordis Webster, Inc.
DRF
Dec 21, 1995K954390CORDIS WESTER STAR CATHETER
Cordis Webster, Inc.
DRF
Nov 22, 1995K953768CORDIS WEBSTER A20 DIAGNOSTIC DEFLECTABLE TIP CATHETER
Cordis Webster, Inc.
DRF

Latest recalls

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