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FDA 510(k)

CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER

K-Number: K023880 · 2002-12-11

ApplicantETHICON, Inc.
Decision Date2002-12-11
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2002-12-11 under 510(k) number K023880. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER?

CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER is a medical device that received FDA 510(k) clearance on 2002-12-11. The listed applicant is ETHICON, Inc.. The 510(k) number is K023880.

When did CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER receive FDA 510(k) clearance?

CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER received FDA 510(k) clearance on 2002-12-11, under 510(k) number K023880.

Who is the listed applicant for CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER?

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

What is the FDA product code for CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER?

The FDA product code for CARDIO VATIONS STEERABLE CORONARY SINUS CATHETER is DWF.

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Related Devices (Code: DWF)

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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.

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