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PMA de la FDA

Sensor, glucose, invasive

Número de PMA: P150029 · 2022-04-29

SolicitanteMedtronic Minimed
Fecha de decisión2022-04-29
Número PMAP150029
Código de productoMDS
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCH

Resumen del dispositivo

Sensor, glucose, invasive is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed. It received FDA 510(k) clearance on 2022-04-29. The device is classified under product code MDS. It was reviewed by the CH advisory panel.

Preguntas frecuentes

What is the Sensor, glucose, invasive?

Sensor, glucose, invasive is a medical device that received FDA 510(k) clearance on 2022-04-29. The listed applicant is Medtronic Minimed.

When did Sensor, glucose, invasive receive FDA 510(k) clearance?

The clearance date for Sensor, glucose, invasive can be found in the official FDA records.

Who is the listed applicant for Sensor, glucose, invasive?

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

What is the FDA product code for Sensor, glucose, invasive?

The FDA product code for Sensor, glucose, invasive is MDS.

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Fuente oficial

Ver en la base de datos de la FDA →

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