FDA PMA

Drug-Eluting Peripheral Transluminal Angioplasty Catheter

Numéro PMA : P140010 · 2026-09-24

DemandeurMedtronic, Inc.

Date de décision2026-09-24

Numéro PMAP140010

Code produitONU

Classe de dispositifClasse 3

Spécialité médicaleU

Comité consultatifCV

Résumé du dispositif

Drug-Eluting Peripheral Transluminal Angioplasty 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 2026-09-24. The device is classified under product code ONU. It was reviewed by the CV advisory panel.

Questions fréquentes

What is the Drug-Eluting Peripheral Transluminal Angioplasty Catheter?

Drug-Eluting Peripheral Transluminal Angioplasty Catheter is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Medtronic, Inc..

When did Drug-Eluting Peripheral Transluminal Angioplasty Catheter receive FDA 510(k) clearance?

The clearance date for Drug-Eluting Peripheral Transluminal Angioplasty Catheter can be found in the official FDA records.

Who is the listed applicant for Drug-Eluting Peripheral Transluminal Angioplasty 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 Drug-Eluting Peripheral Transluminal Angioplasty Catheter?

The FDA product code for Drug-Eluting Peripheral Transluminal Angioplasty Catheter is ONU.

Essais cliniques associés

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Source officielle

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