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Premarket approval / Center for Devices and Radiological Health / Title 21 of the Code of Federal Regulations / Hirudo medicinalis / Leech / Quality management system / Anticoagulant / Medical device / Federal Food / Drug / and Cosmetic Act / Medicine / Food and Drug Administration / Health


JUN[removed]k) Summary Date Prepared: January 15, [removed].
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Document Date: 2004-07-14 11:57:22

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File Size: 108,27 KB

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