Before using the Mako system, each end effector had established a specific number sequence to help the Mako system establish a tool control point (TCP) for each tool assembled to the end effector. On the handle of the eccentric acetabular file, each orientation slot of 45 degrees, 90 degrees...
The numbers demonstrate the Food and Drug Administration's inability to control the tumultuous vaping market more than three years afterdeclaring a crackdown on kid-friendly flavors. Most of the disposable e-cigarettes, which are thrown away after they're used up, come in sweet and fruity flavors...
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SPL-formatted drug labels; NDC numbers with the related information on drugs marketed in the US; and data on drug recalls, or events when certain medications are removed from the market. All APIs return responses in JSON format. It’s worth noting that not all information provided by openFDA...
“Common side effects of blood thinners, like bruising and increased bleeding, are significant concerns,” Sazan Sylejmani, owner and pharmacy manager at Westmont Pharmacy in Westmont, Ill., told Drugwatch. “Patients can minimize these risks by using soft toothbrushes and electric razors and ...
Karan recalls working with one client selling a device that projected an image of the night sky on walls and ceilings. “We got a utility patent on the actual device, the hardware elements; and we also got a patent on the exterior of the device,” he says. “It was very distinct in...
The person is an IV drug abuser. The person is on steroid therapy, chemotherapy, other drugs that suppress the immune system, or dialysis. The sore is located at the top of the buttock crease, or it is on or near the rectal or groin area. ...
Error Types and Associations of Clinically Significant Events within FDA Recalls of Linear Accelerators and Related ProductsPurpose: Medical devices in radiation therapy undergo a complex process of Food and Drug Administration (FDA) approval. Little is known about which processes within the radiation ...
Performance bias occurs mainly in medical research experiments, if participants have knowledge of the planned intervention, therapy, or drug trial before it begins. Studies about nutrition, exercise outcomes, or surgical interventions are very susceptible to this type of bias. It can be minimized by...
Medical device recalls and the FDA approval process. BACKGROUND: Unlike prescription drugs, medical devices are reviewed by the US Food and Drug Administration (FDA) using 2 alternative regulatory standards: ... DM Zuckerman,P Brown,SE Nissen - 《Archives of Internal Medicine》 被引量: 337发表...