Sectra-Imtec AB - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Sectra-Imtec AB has 14 FDA 510(k) cleared radiology devices. Based in Aubrey, US.
Historical record: 14 cleared submissions from 1996 to 2011.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Apr 28, 2011
SECTRA MICRODOSE MAMMOGRAPHY
Radiology
115d
Cleared
Jun 12, 2008
SECTRA WORKSTATION, IDS7 VERSION 11.3, IDS5 VERSION 11.1 P2
Radiology
16d
Cleared
Nov 07, 2006
SECTRA WORKSTATION, VERSION 11.1
Radiology
28d
Cleared
Jun 15, 2005
MODIFICATION TO: SECTRA IDS5 WORKSTATION
Radiology
26d
Cleared
Feb 24, 2005
SECTRA IDS5 WORKSTATION
Radiology
28d
Cleared
May 04, 2004
SECTRA IDS5 RADIOLOGY WORKSTATION
Radiology
77d
Cleared
Dec 23, 2003
MODIFICATION TO SECTRA IDS5 RADIOLOGY WORKSTATION - VERSION 10.1
Radiology
27d
Cleared
Oct 02, 2003
SECTRA ORTHOPEDIC PACKAGE
Radiology
134d
Cleared
Jun 07, 2002
SECTRA OSTEOPOROSIS PACKAGE
Radiology
28d
Cleared
Oct 17, 2000
MODIFICATION TO IDS5 IMAGE DISPLAY SYSTEM
Radiology
26d
Cleared
Oct 29, 1998
WISE (II) IMAGE MANAGEMENT SYSTEM
Radiology
29d
Cleared
Mar 12, 1997
SMIIC (SECTRA MEDICAL IMAGE INPUT CONTROLLER)
Radiology
79d