510(k) SUMMARY (as required by[removed]c[removed]JUL

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Date: 2012-08-06 18:53:43 Technology Medical device Center for Devices and Radiological Health Premarket approval Federal Food Drug and Cosmetic Act Infusion set Title 21 of the Code of Federal Regulations Quality management system Subcutaneous injection Medicine Food and Drug Administration Health		510(k) SUMMARY (as required by[removed]c[removed]JUL Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 123,75 KB Share Document on Facebook

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