510(k) Summary Date Submitted: 3 2012

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Date: 2012-08-06 18:53:12 Medical device Federal Food Drug and Cosmetic Act Premarket approval Remote patient monitoring Center for Devices and Radiological Health Health care Medicine Health Food and Drug Administration		510(k) Summary Date Submitted: 3 2012 Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 173,48 KB Share Document on Facebook

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