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PMA de la FDA

Computer-assisted personalized sedation system

Número de PMA: P080009 · 2016-03-15

SolicitanteScott Laboratories, Inc.
Fecha de decisión2016-03-15
Número PMAP080009
Código de productoPDR
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorAN

Resumen del dispositivo

Computer-assisted personalized sedation system is the device name listed in this FDA 510(k) record. The listed applicant is Scott Laboratories, Inc.. It received FDA 510(k) clearance on 2016-03-15. The device is classified under product code PDR. It was reviewed by the AN advisory panel.

Preguntas frecuentes

What is the Computer-assisted personalized sedation system?

Computer-assisted personalized sedation system is a medical device that received FDA 510(k) clearance on 2016-03-15. The listed applicant is Scott Laboratories, Inc..

When did Computer-assisted personalized sedation system receive FDA 510(k) clearance?

The clearance date for Computer-assisted personalized sedation system can be found in the official FDA records.

Who is the listed applicant for Computer-assisted personalized sedation system?

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

What is the FDA product code for Computer-assisted personalized sedation system?

The FDA product code for Computer-assisted personalized sedation system is PDR.

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Fuente oficial

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