K131493 p.1 of 4 Page 1 Traditional 510(k)

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Date: 2013-09-13 12:40:40 Medical equipment Food and Drug Administration Percutaneous Port Premarket approval Federal Food Drug and Cosmetic Act Medical device Remote magnetic navigation Central venous catheter Medicine Medical technology Catheters		K131493 p.1 of 4 Page 1 Traditional 510(k) Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 180,72 KB Share Document on Facebook

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