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Medtronic Defibrillator Lead Recall Attorneys

Medtronic gets FDA Approval for CGMS iPRO

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Editor: Marc Jay Bern
Profession: Defective Medical Device Lawyer

January 29, 2008

By Marc Bern

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Category: Medtronic News

On Tuesday, Medtronic announced they have received approval from the Food and Drug Administration (FDA) for its GMS iPro Recorder, a continuous glucose monitoring system.

The GMS iPro is used to analyze how everyday activities can interfere and affect a patient's diabetes management.

For three days patients wear the iPro recorder. The device allows physicians to review the data recorded over the three days and use the results to determine glucose patterns which allow them to optimize patient therapy.


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