FDA reclassifies certain digital mammography devices today

by FDA on November 4, 2010

in FDA Alerts

Devices capturing digital image of breasts to be Class II. The U.S. Food and Drug Administration today announced that it is easing the pathway to market for mammography systems that produce computerized X-ray images of the entire breast.

This is a summary of a Press Release issued by the Food and Drug Administration (FDA). The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.

View Full Details Of Original FDA Press Release Here.

Bookmark and Share

Leave a Comment

Previous post:

Next post: