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PMA de la FDA

Pump, infusion, implanted, programmable

Número de PMA: P140032 · 2021-08-31

SolicitanteMedtronic, Inc.
Fecha de decisión2021-08-31
Número PMAP140032
Código de productoLKK
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorHO

Resumen del dispositivo

Pump, infusion, implanted, programmable is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2021-08-31. The device is classified under product code LKK. It was reviewed by the HO advisory panel.

Preguntas frecuentes

What is the Pump, infusion, implanted, programmable?

Pump, infusion, implanted, programmable is a medical device that received FDA 510(k) clearance on 2021-08-31. The listed applicant is Medtronic, Inc..

When did Pump, infusion, implanted, programmable receive FDA 510(k) clearance?

The clearance date for Pump, infusion, implanted, programmable can be found in the official FDA records.

Who is the listed applicant for Pump, infusion, implanted, programmable?

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

What is the FDA product code for Pump, infusion, implanted, programmable?

The FDA product code for Pump, infusion, implanted, programmable is LKK.

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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