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PMA de la FDA

Aspiration therapy system

Número de PMA: P150024 · 2020-04-24

SolicitanteAspire Bariatrics, Inc.
Fecha de decisión2020-04-24
Número PMAP150024
Código de productoOYF
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorGU

Resumen del dispositivo

Aspiration therapy system is the device name listed in this FDA 510(k) record. The listed applicant is Aspire Bariatrics, Inc.. It received FDA 510(k) clearance on 2020-04-24. The device is classified under product code OYF. It was reviewed by the GU advisory panel.

Preguntas frecuentes

What is the Aspiration therapy system?

Aspiration therapy system is a medical device that received FDA 510(k) clearance on 2020-04-24. The listed applicant is Aspire Bariatrics, Inc..

When did Aspiration therapy system receive FDA 510(k) clearance?

The clearance date for Aspiration therapy system can be found in the official FDA records.

Who is the listed applicant for Aspiration therapy system?

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

What is the FDA product code for Aspiration therapy system?

The FDA product code for Aspiration therapy system is OYF.

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Fuente oficial

Ver en la base de datos de la FDA →

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