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PMA de la FDA

heart-valve, non-allograft tissue

Número de PMA: P060038 · 2019-11-21

SolicitanteCorcym Canada Corp
Fecha de decisión2019-11-21
Número PMAP060038
Código de productoLWR
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

heart-valve, non-allograft tissue is the device name listed in this FDA 510(k) record. The listed applicant is Corcym Canada Corp. It received FDA 510(k) clearance on 2019-11-21. The device is classified under product code LWR. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the heart-valve, non-allograft tissue?

heart-valve, non-allograft tissue is a medical device that received FDA 510(k) clearance on 2019-11-21. The listed applicant is Corcym Canada Corp.

When did heart-valve, non-allograft tissue receive FDA 510(k) clearance?

The clearance date for heart-valve, non-allograft tissue can be found in the official FDA records.

Who is the listed applicant for heart-valve, non-allograft tissue?

The FDA 510(k) record lists Corcym Canada Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for heart-valve, non-allograft tissue?

The FDA product code for heart-valve, non-allograft tissue is LWR.

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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.

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