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FDA Seeks More Comments on Lasik

Agency extends deadline for submission of public comments on popular laser vision correction surgery.


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Public opinions about Lasik sought by US Food and Drug Administration

ROCKVILLE, Maryland, November 17, 2009, /FDA/ -- The US Food and Drug Administration (FDA) is extending its request for public information and comments on Lasik, according to a notice published in the Federal Register. The FDA will accept comments until Nov. 15, 2010.

"At this time, the agency is reopening the docket to continue to receive public comments," reports the notice. "Information and comments submitted to the docket will assist us in identifying ways in which we can improve our public outreach efforts regarding the safety and effectiveness of LASIK devices."

Comments or information can be submitted at www.regulations.gov or sent to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. The docket number - FDA-2008-N-0488 - must be included with submitted comments.


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