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26 Sep 2017, 7:00 am
In the United States, the Food and Drug Administration reported that by 2018, approximately 1.7 billion smartphone users around the world will be using a medical mobile app. [read post]
20 Dec 2016, 5:00 am
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
9 Feb 2012, 9:43 am
Food and Drug Administration, the FDA sent a letter to the corporation warning the company that the implants were potentially hazardous, and cited 11 ways in which the business’ production process deviated from acceptable manufacturing standards. [read post]
20 Feb 2017, 12:28 pm
According to the Food and Drug Administration, as of 2012, about 324,200 people worldwide have received cochlear implants, and more than 26 percent of recipients lived in the United States. [read post]
19 Jan 2016, 6:41 am
Your lawyer will need an expert witness who is familiar with the requirements of the United States Food and Drug Administration (FDA) that pertain to medical devices, as well as having knowledge of production techniques and medical device marketing regulations. [read post]
25 May 2007, 6:33 am
Methods: All preoperative and postoperative radiographs from a completed prospective, randomized, United States Food and Drug Administration-regulated trial comparing replacement with the CHARITÉ Artificial Disc with anterior interbody arthrodesis were analyzed. [read post]
20 Dec 2016, 5:00 am
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
19 Nov 2021, 6:08 am
In June of 2021, the United States Food and Drug Administration (FDA) issued a recall of millions of Philips CPAP, BiPAP, and ventilator machines. [read post]
15 Jun 2012, 3:52 pm
In 2008, the United States Food and Drug Administration (“FDA”) issued a Public Health Notification (“PHN”) to warn patients about adverse effects related to urogynecologic use of surgical mesh. [read post]
26 May 2011, 5:14 pm
Food and Drug Administration’s (FDA) 510(k) approval process, which allows a medical device to be placed on the market without being subjected to clinical trials as long as the manufacturer can show that the device is “substantially equivalent” to a device already approved on the market. [read post]
15 Jun 2012, 3:52 pm
In 2008, the United States Food and Drug Administration (“FDA”) issued a Public Health Notification (“PHN”) to warn patients about adverse effects related to urogynecologic use of surgical mesh. [read post]
26 Jul 2012, 1:37 pm
FDA Adverse Effects Reports The Food and Drug Administration has received more than 3,800 reports of significant complications associated with transvaginal mesh patches. [read post]
28 Jun 2013, 3:23 am
A focus on plaque For Devous, the game changer came last year with the Food and Drug Administration’s approval of Amyvid, an amyloid imaging agent that allows researchers to track plaque in positron emission tomography scans. [read post]
2 Jul 2016, 9:03 am
Guidance from the Food and Drug Administration (FDA) and the Centers for Disease Control (CDC) continues to warn that consumers should refrain from consuming any raw products made with flour. [read post]
19 May 2010, 11:00 am
Although research is ongoing, the Food and Drug Administration (FDA) says that available scientific evidence--including World Health Organization (WHO) findings released May 17, 2010--shows no increased health risk due to radiofrequency (RF) energy, a form of electromagnetic radiation that is emitted by cell phones. [read post]
21 Sep 2018, 8:46 am
Companies in the United States and Europe are expected to begin treating patients with CRISPR-based therapies this year. [read post]
24 Dec 2011, 4:02 am
Food and Drug Administration launched a new initiative to prevent surgical fires, noting that although these flash fires are relatively rare events, they are also highly preventable. [read post]
19 Nov 2021, 6:08 am
In June of 2021, the United States Food and Drug Administration (FDA) issued a recall of millions of Philips CPAP, BiPAP, and ventilator machines. [read post]
30 Jun 2010, 9:00 am
Kellogg Company Voluntarily Recalls Select Packages ofKellogg's® Corn Pops®, Kellogg's® Honey Smacks®, Kellogg's® Froot Loops® and Kellogg's® Apple Jacks® Working in consultation with the United States Food and Drug Administration (FDA), Kellogg Company (NYSE:K) is implementing a voluntary recall of certain breakfast cereals due to an uncharacteristic off-flavor and smell coming from the liner… [read post]
28 Dec 2011, 7:07 am
DePuy recalled the defective hip implants after the Food and Drug Administration (FDA) received about 400 complaints in two years from patients. [read post]
