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FDA PMA

Permanent defibrillator electrodes

PMA Number: P920015 · 2026-08-19

ApplicantMedtronic, Inc.
Decision Date2026-08-19
PMA NumberP920015
Product CodeNVY
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeCV

Device Summary

Permanent defibrillator electrodes is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2026-08-19. The device is classified under product code NVY. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Permanent defibrillator electrodes?

Permanent defibrillator electrodes is a medical device that received FDA 510(k) clearance on 2026-08-19. The listed applicant is Medtronic, Inc..

When did Permanent defibrillator electrodes receive FDA 510(k) clearance?

The clearance date for Permanent defibrillator electrodes can be found in the official FDA records.

Who is the listed applicant for Permanent defibrillator electrodes?

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 Permanent defibrillator electrodes?

The FDA product code for Permanent defibrillator electrodes is NVY.

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.

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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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