Sentence examples for devices for clearing from inspiring English sources

The university specialises in defence and security studies, or what it describes as issues of "resilience", covering a range of areas from an organisation's vulnerability to terrorist attacks or the best options for using explosive devices for clearing mines, to research programmes including disaster management and missile control systems.

You also characterized the F.D.A.'s 510(k) process for clearing new medical devices as "cursory".

For instance, small tele-operated vehicles are used for clearing improvised explosive devices, known as I.E.D.'s, and for some surveillance tasks.

The end of what was called "selective availability" to information from satellites improved the accuracy of devices for users worldwide, clearing the way for millions of drivers, dolts included, to purchase them.

The injuries may stem from the fact that far too many medical devices are cleared for sale without undergoing rigorous clinical trials for safety and efficacy.

Unlike prescription drugs, many medical devices are cleared for sale by the Food and Drug Administration without extensive studies in patients.

A prestigious medical group is concerned that most medical devices are cleared for sale without evidence that they are safe and effective.

Morcellators came onto the market in 1991 via an F.D.A. process known as 510 k), in which devices are cleared for use without going through the usual lengthy approval process, because they are similar to devices that have already been approved.

No wonder many patient advocates cheered when the FDA announced in November that it planned to make "transformative" changes in the way more than 80percentt of medical devices are cleared for sale in the United States.

Currently, the vast majority of medical devices are cleared for marketing without clinical testing or weighty evidence that they are safe and effective; a manufacturer simply has to show that its device is "substantially equivalent" to one that has previously been cleared — even if the earlier device was recalled by the manufacturer after safety problems.

Under this provision, known as the 510(k) pathway, new artificial joints, cataract lens implants and thousands of other devices developed after 1976 can win approval for sale (or "clearance" in FDA parlance) if the product is shown to have "substantial equivalence" to a previously cleared "predicate" device". Four out of five devices are cleared for sale this way.