FDA 510(k) Applications Submitted by SECTRA IMTEC AB

FDA 510(k) Number	Submission Date	Device Name	Applicant
K110025	01/03/2011	SECTRA MICRODOSE MAMMOGRAPHY	SECTRA IMTEC AB
K081469	05/27/2008	SECTRA WORKSTATION, IDS7 VERSION 11.3, IDS5 VERSION 11.1 P2	SECTRA IMTEC AB
K050196	01/27/2005	SECTRA IDS5 WORKSTATION	SECTRA IMTEC AB
K051315	05/20/2005	MODIFICATION TO: SECTRA IDS5 WORKSTATION	SECTRA IMTEC AB
K063093	10/10/2006	SECTRA WORKSTATION, VERSION 11.1	SECTRA IMTEC AB