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FDA PMA

Cardiac ablation percutaneous catheter

PMA Number: P930029 · 2024-07-01

Decision Date2024-07-01
PMA NumberP930029
Product CodeLPB
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Cardiac ablation percutaneous catheter is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2024-07-01. The device is classified under product code LPB. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Cardiac ablation percutaneous catheter?

Cardiac ablation percutaneous catheter is a medical device that received FDA 510(k) clearance on 2024-07-01. The listed applicant is Medtronic, Inc..

When did Cardiac ablation percutaneous catheter receive FDA 510(k) clearance?

The clearance date for Cardiac ablation percutaneous catheter can be found in the official FDA records.

Who is the listed applicant for Cardiac ablation percutaneous catheter?

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

What is the FDA product code for Cardiac ablation percutaneous catheter?

The FDA product code for Cardiac ablation percutaneous catheter is LPB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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