FDA PMA

Sensor, glucose, invasive

Número do PMA: P980022 · 2019-08-14

RequerenteMedtronic Minimed

Data da decisão2019-08-14

Número PMAP980022

Código do produtoMDS

Classe do DispositivoClasse 3

Especialidade MédicaU

Comité consultivoCH

Resumo do 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 2019-08-14. The device is classified under product code MDS. It was reviewed by the CH advisory panel.

Perguntas frequentes

What is the Sensor, glucose, invasive?

Sensor, glucose, invasive is a medical device that received FDA 510(k) clearance on 2019-08-14. 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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