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Hemoperfusion
Results: 5

#	Item
1	Gastroenterology-Urology Devices Panel Session I June 27, 2013 Gastroenterology-Urology Devices Panel Meeting June 27, 2013 Add to Reading List Source URL: www.fda.gov Language: English Transfusion medicine Health Pharmaceutical sciences Poison Food and Drug Administration Medicine Hemoperfusion Renal dialysis
2	FDA Executive Summary Prepared for the June 27, 2013 meeting of the Gastroenterology and Urology Devices Panel Classification of Sorbent Hemoperfusion Systems Add to Reading List Source URL: www.fda.gov Language: English Hemoperfusion Premarket approval Medical device Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Medicine Food and Drug Administration Health
3	Classification and Regulation of Sorbent Hemoperfusion Systems 21 CFR §[removed]Gema Gonzalez, MS Division of Reproductive, Gastro-Renal, and Urological Devices Add to Reading List Source URL: www.fda.gov Language: English Hemoperfusion Transfusion medicine Dialysis Activated carbon Medical device Food and Drug Administration Hemodialysis Medicine Renal dialysis Membrane technology
4	FDA has identified the following risks to health for implanted blood access devices for hemodialysis based on the input of the original classification panel, review of industry responses to the[removed]i) order, the Man Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Food law Pharmaceuticals policy Medical device Medical technology Hemoperfusion Adverse effect Federal Food Drug and Cosmetic Act Risk assessment Medicine Health Pharmacology
5	Classification and Regulation of Sorbent Hemoperfusion Systems 21 CFR §[removed] Add to Reading List Source URL: www.fda.gov Language: English Electrolyte Physical chemistry Potassium chloride Machine perfusion Battery PH Chemistry Chlorides Dietary minerals

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