Devices, drugs, and the Food and Drug Administration:... [Stroke. 2005] - PubMed

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The Food and Drug Administration medical device review process: clearance of a clot retriever for use in ischemic stroke. [Stroke. 2005]
The Food and Drug Administration medical device review process: clearance of a clot retriever for use in ischemic stroke.
Felten RP, Ogden NR, Peña C, Provost MC, Schlosser MJ, Witten CM. Stroke. 2005 Feb; 36(2):404-6. Epub 2004 Dec 29.
Review An example of US Food and Drug Administration device regulation: medical devices indicated for use in acute ischemic stroke. [Stroke. 2007]
Review An example of US Food and Drug Administration device regulation: medical devices indicated for use in acute ischemic stroke.
Peña C, Li K, Felten R, Ogden N, Melkerson M. Stroke. 2007 Jun; 38(6):1988-92. Epub 2007 May 3.
Approval of the MERCI clot retriever: a critical view. [Stroke. 2005]
Approval of the MERCI clot retriever: a critical view.
Becker KJ, Brott TG. Stroke. 2005 Feb; 36(2):400-3. Epub 2005 Jan 13.
Devices and drugs for stroke: why do regulations differ? [Lancet Neurol. 2009]
Devices and drugs for stroke: why do regulations differ?
Mayor S. Lancet Neurol. 2009 Nov; 8(11):982-3.
Review Review of the processes for FDA oversight of drugs, medical devices, and combination products. [J Manag Care Pharm. 2011]
Review Review of the processes for FDA oversight of drugs, medical devices, and combination products.
Sweet BV, Schwemm AK, Parsons DM. J Manag Care Pharm. 2011 Jan-Feb; 17(1):40-50.

Critical appraisal of medical devices in the management of cerebrovascular disease. [Ther Clin Risk Manag. 2008]
Critical appraisal of medical devices in the management of cerebrovascular disease.
Schneck MJ. Ther Clin Risk Manag. 2008 Feb; 4(1):19-29.

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