510(k) Summary Submission Date: 17 December[removed]Submitter

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Date: 2011-04-25 00:30:46 Health Food law Medical equipment Pharmaceutical industry Medical technology Medical device Premarket approval Validation Title 21 of the Code of Federal Regulations Medicine Food and Drug Administration Technology		510(k) Summary Submission Date: 17 December[removed]Submitter Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 196,98 KB Share Document on Facebook

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