PMA de la FDA

STENT, CORONARY

Número de PMA: P110004 · 2020-04-09

SolicitanteMedinol, Ltd.

Fecha de decisión2020-04-09

Número PMAP110004

Código de productoMAF

Clase del dispositivoClase 3

Especialidad médicaU

Comité asesorCV

Resumen del dispositivo

STENT, CORONARY is the device name listed in this FDA 510(k) record. The listed applicant is Medinol, Ltd.. It received FDA 510(k) clearance on 2020-04-09. The device is classified under product code MAF. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the STENT, CORONARY?

STENT, CORONARY is a medical device that received FDA 510(k) clearance on 2020-04-09. The listed applicant is Medinol, Ltd..

When did STENT, CORONARY receive FDA 510(k) clearance?

The clearance date for STENT, CORONARY can be found in the official FDA records.

Who is the listed applicant for STENT, CORONARY?

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

What is the FDA product code for STENT, CORONARY?

The FDA product code for STENT, CORONARY is MAF.

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.