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PMA de la FDA

Processor, cervical cytology slide, automated

Número de PMA: P970018 · 2024-09-06

SolicitanteBd Diagnostic Systems
Fecha de decisión2024-09-06
Número PMAP970018
Código de productoMKQ
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorPA

Resumen del dispositivo

Processor, cervical cytology slide, automated is the device name listed in this FDA 510(k) record. The listed applicant is Bd Diagnostic Systems. It received FDA 510(k) clearance on 2024-09-06. The device is classified under product code MKQ. It was reviewed by the PA advisory panel.

Preguntas frecuentes

What is the Processor, cervical cytology slide, automated?

Processor, cervical cytology slide, automated is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Bd Diagnostic Systems.

When did Processor, cervical cytology slide, automated receive FDA 510(k) clearance?

The clearance date for Processor, cervical cytology slide, automated can be found in the official FDA records.

Who is the listed applicant for Processor, cervical cytology slide, automated?

The FDA 510(k) record lists Bd Diagnostic Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Processor, cervical cytology slide, automated?

The FDA product code for Processor, cervical cytology slide, automated is MKQ.

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Fuente oficial

Ver en la base de datos de la FDA →

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