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	921.	Medical devices; effective date of requirement for premarket approval for three class III preamendments devices. Final rule. [electronic resource] Producer: 20040707 In: Federal register vol. 69 Availability: No items available. Save to lists Add to cart (remove)
	922.	Peanut test kits approved. [electronic resource] Producer: 20040413 In: FDA consumer vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	923.	Medical Device Manufacturing and Medical Device Reports (MDR). [electronic resource] by Arellano, Veronica Producer: 20091112 In: Insight (American Society of Ophthalmic Registered Nurses) vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	924.	FDA is gold standard of review. [electronic resource] by Leahey, Mark B Producer: 20110118 In: BMJ (Clinical research ed.) vol. 341 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	925.	Cardiovascular devices; reclassification of certain percutaneous transluminal coronary angioplasty (PTCA) catheters. Final rule. [electronic resource] Producer: 20101001 In: Federal register vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	926.	Postmarket Modifications of High-Risk Therapeutic Devices in Otolaryngology Cleared by the US Food and Drug Administration. [electronic resource] by Rathi, Vinay K Ross, Joseph S Samuel, Andre M Mehra, Saral Producer: 20151127 In: Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	927.	Medical devices; neurological devices; classification of the limited output transcutaneous piezoelectric stimulator for skin reactions associated with insect bites. Final order. [electronic resource] Producer: 20150429 In: Federal register vol. 80 Availability: No items available. Save to lists Add to cart (remove)
	928.	Regulatory reticence and medical devices. [electronic resource] by Fox, Daniel M Zuckerman, Diana M Producer: 20140428 In: The Milbank quarterly vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	929.	Testing devices for the prevention and treatment of stroke and its complications. [electronic resource] by Bath, Philip M Brainin, Michael Brown, Chloe Campbell, Bruce Davis, Stephen M Donnan, Geoffrey A Ford, Gary A Hacke, Werner Iglesias, Cynthia Lees, Kennedy R Pugh, Stacey S Saver, Jeff L Schellinger, Peter D Truelsen, Thomas Producer: 20150330 In: International journal of stroke : official journal of the International Stroke Society vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	930.	Medical Devices; Obstetrical and Gynecological Devices; Classification of the Gynecologic Laparoscopic Power Morcellation Containment System. Final order. [electronic resource] Producer: 20160624 In: Federal register vol. 81 Availability: No items available. Save to lists Add to cart (remove)
	931.	US device industry and FDA "colluded" on legislation to weaken regulatory oversight. [electronic resource] by Lenzer, Jeanne Producer: 20160310 In: BMJ (Clinical research ed.) vol. 351 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	932.	The Role of the FDA in Ensuring the Safety and Efficacy of Artificial Intelligence Software and Devices. [electronic resource] by Allen, Bibb Producer: 20190802 In: Journal of the American College of Radiology : JACR vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	933.	Implementation of ST-segment criteria in clinical monitoring devices. Implications of criteria from field trials and the federal regulatory process. [electronic resource] by Kotilainen, P W Producer: 19950413 In: Journal of electrocardiology vol. 27 Suppl Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	934.	Market briefing: 'dollars and stents': new technology will have major impact on heart care. [electronic resource] Producer: 20030205 In: Russ Coile's health trends vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	935.	Making medical progress. A look at FDA approvals in 2000. [electronic resource] Producer: 20010712 In: FDA consumer vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	936.	Replacement parts. How the FDA allows faulty, and sometimes dangerous, medical devices onto the market. [electronic resource] by Roane, Kit R Producer: 20020822 In: U.S. news & world report vol. 133 Availability: No items available. Save to lists Add to cart (remove)
	937.	FDA modernization act of 1997: guidance on medical device tracking; availability--FDA. Notice. [electronic resource] Producer: 19980428 In: Federal register vol. 63 Availability: No items available. Save to lists Add to cart (remove)
	938.	FDA spells out new reporting requirements. [electronic resource] by Infante, M Producer: 19960502 In: Contemporary longterm care vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	939.	Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, distributor reporting. Food and Drug Administration, HHS. Final rule. [electronic resource] Producer: 20000922 In: Federal register vol. 65 Availability: No items available. Save to lists Add to cart (remove)
	940.	Will new FDA rules hasten device approval? [electronic resource] Producer: 20030821 In: Hospital material[dollar sign] management vol. 28 Availability: No items available. Save to lists Add to cart (remove)

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