FDA 510(k)

CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER

K-Number: K955817 · 1996-03-25

Decision Date1996-03-25

Product CodeDRF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Webster, Inc.. It received FDA 510(k) clearance on 1996-03-25 under 510(k) number K955817. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER?

CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER is a medical device that received FDA 510(k) clearance on 1996-03-25. The listed applicant is Cordis Webster, Inc.. The 510(k) number is K955817.

When did CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER receive FDA 510(k) clearance?

CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER received FDA 510(k) clearance on 1996-03-25, under 510(k) number K955817.

Who is the listed applicant for CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER?

The FDA 510(k) record lists Cordis Webster, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER?

The FDA product code for CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETER is DRF.

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Other records listing Cordis Webster, Inc. as applicant

K992965CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085 K991531CORDIS WEBSTER DIAGNOSTIC DEFLECTABLE TIP CATHETER, MODEL D-1078 K982740CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL #'S 301-803A, 301-803P, 301-803M, 301-813S K982415CORDIS WEBSTER REF-STAR EXTERNAL REFERENCE PATCH, MODEL # D-1210 K980961CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.K970264CORDIS WEBSTER BRAIDED GUIDING SHEATH EXCHANGE SYSTEM

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Related Devices (Code: DRF)

K252794Vision-MR™ Diagnostic CatheterImricor Medical Systems, Inc.K250590MAGiC Sweep™ EP Mapping CatheterStereotaxis, Inc.K250310VIKING™ Fixed Curve Diagnostic CatheterBoston Scientific Corporation K240366EP•XT™ Unidirectional Steerable Diagnostic Catheter; Dynamic Tip™ Unidirectional Steerable Diagnostic Catheter; Dynamic XT™ Unidirectional Steerable Diagnostic CatheterBoston Scientific Corporation K233900Nordica PV Cryo Mapping CatheterSynaptic Medical Corporation K233397Cosine-10TM Diagnostic CatheterMedtronic, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.