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Risk Management: Page 19
More NIH research funds could aid imaging effort
By
Roger Lindahl
The effort to establish a separate imaging institute at the National Institutes of Health (NIH) could get a boost after President Bill Clinton announced that he will be asking Congress for a substantial increase in fiscal 2001 funding for research at the
January 24, 2000
FDA approves more MQSA info; begins search engine update
By
Tracie L. Thompson
Does mammography experience acquired outside the U.S. count toward the requirements of the Mammography Quality Standards Act? That's just one of the questions answered in the latest guidelines finalized by the FDA's Center for Devices and Radiological Hea
January 20, 2000
FDA takes steps to examine reuse of catheters, devices
By
Shalmali Pal
The Food and Drug Administration has moved one step closer to implementing guidelines for medical device reprocessors.
December 22, 1999
CTI makes progress with thermal PMA
By
AuntMinnie.com staff writers
December 19, 1999
FDA panel votes to recommend GE digital mammo unit
By
Brian Casey
A Food and Drug Administration advisory panel voted unanimously Dec. 16 to recommend approval of a full-field digital mammography system developed by GE Medical Systems.
December 16, 1999
FDA panel to review GE's digital mammography system
By
Brian Casey
A Food and Drug Administration advisory panel is meeting today to review a premarket approval (PMA) application filed by GE Medical Systems of Waukesha, WI, for a full-field digital mammography system.
December 15, 1999
Peak to build exam beds for CTI system
By
AuntMinnie.com staff writers
December 14, 1999
Alliance files NDA for Imagent contrast
By
AuntMinnie.com staff writers
December 14, 1999
FDA scrutinizes reuse of single-use devices
By
Shalmali Pal
Medical device manufacturers faced off in Maryland on Dec. 14 over the issue of reprocessing single-use devices at a public forum hosted by the Food and Drug Administration.
December 13, 1999
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