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PMA de la FDA

Automated external defibrillators (non-wearable)

Número de PMA: P160034 · 2020-03-01

SolicitanteZOLL Medical Corporation
Fecha de decisión2020-03-01
Número PMAP160034
Código de productoMKJ
Clase del dispositivoClase 3
Especialidad médicaC
Número de regulación21 CFR 8
Comité asesorCV

Resumen del dispositivo

Automated external defibrillators (non-wearable) is the device name listed in this FDA 510(k) record. The listed applicant is ZOLL Medical Corporation. It received FDA 510(k) clearance on 2020-03-01. The device is classified under product code MKJ. It was reviewed by the CV advisory panel. Product code MKJ falls under the category of Dental, which includes dental instruments, materials, and equipment. Devices in this category are subject to specific FDA regulatory requirements.

Preguntas frecuentes

What is the Automated external defibrillators (non-wearable)?

Automated external defibrillators (non-wearable) is a medical device that received FDA 510(k) clearance on 2020-03-01. The listed applicant is ZOLL Medical Corporation.

When did Automated external defibrillators (non-wearable) receive FDA 510(k) clearance?

The clearance date for Automated external defibrillators (non-wearable) can be found in the official FDA records.

Who is the listed applicant for Automated external defibrillators (non-wearable)?

The FDA 510(k) record lists ZOLL Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Automated external defibrillators (non-wearable)?

The FDA product code for Automated external defibrillators (non-wearable) is MKJ. This falls under the Dental category.

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Fuente oficial

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