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PMA de la FDA

implanted diaphragmatic/phrenic nerve Stimulator

Número de PMA: P860026 · 2019-11-04

SolicitanteAvery Biomedical Devices, Inc.
Fecha de decisión2019-11-04
Número PMAP860026
Código de productoGZE
Clase del dispositivoClase 3
Especialidad médicaN
Número de regulación21 CFR 8
Comité asesorAN

Resumen del dispositivo

implanted diaphragmatic/phrenic nerve Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Avery Biomedical Devices, Inc.. It received FDA 510(k) clearance on 2019-11-04. The device is classified under product code GZE. It was reviewed by the AN advisory panel.

Preguntas frecuentes

What is the implanted diaphragmatic/phrenic nerve Stimulator?

implanted diaphragmatic/phrenic nerve Stimulator is a medical device that received FDA 510(k) clearance on 2019-11-04. The listed applicant is Avery Biomedical Devices, Inc..

When did implanted diaphragmatic/phrenic nerve Stimulator receive FDA 510(k) clearance?

The clearance date for implanted diaphragmatic/phrenic nerve Stimulator can be found in the official FDA records.

Who is the listed applicant for implanted diaphragmatic/phrenic nerve Stimulator?

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

What is the FDA product code for implanted diaphragmatic/phrenic nerve Stimulator?

The FDA product code for implanted diaphragmatic/phrenic nerve Stimulator is GZE.

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Fuente oficial

Ver en la base de datos de la FDA →

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