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FDA 510(k)

LIVEWIRE ELECTOPHYSIOLOGY CATHETER

K-Number: K102721 · 2010-10-18

ApplicantSt Jude Medical
Decision Date2010-10-18
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIVEWIRE ELECTOPHYSIOLOGY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is St Jude Medical. It received FDA 510(k) clearance on 2010-10-18 under 510(k) number K102721. 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 LIVEWIRE ELECTOPHYSIOLOGY CATHETER?

LIVEWIRE ELECTOPHYSIOLOGY CATHETER is a medical device that received FDA 510(k) clearance on 2010-10-18. The listed applicant is St Jude Medical. The 510(k) number is K102721.

When did LIVEWIRE ELECTOPHYSIOLOGY CATHETER receive FDA 510(k) clearance?

LIVEWIRE ELECTOPHYSIOLOGY CATHETER received FDA 510(k) clearance on 2010-10-18, under 510(k) number K102721.

Who is the listed applicant for LIVEWIRE ELECTOPHYSIOLOGY CATHETER?

The FDA 510(k) record lists St Jude Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIVEWIRE ELECTOPHYSIOLOGY CATHETER?

The FDA product code for LIVEWIRE ELECTOPHYSIOLOGY CATHETER is DRF.

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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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