St. Jude Medical Systems AB is one of 57 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
St. Jude Medical Systems AB - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
St. Jude Medical Systems AB has 5 FDA 510(k) cleared medical devices. Based in Uppsala, SE.
Historical record: 5 cleared submissions from 2011 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by St. Jude Medical Systems AB Filter by specialty or product code using the sidebar.
St. Jude Medical Systems AB — FDA 510(k) Products and Clearance History
5 devices
Cleared
Nov 13, 2014
PRESSUREWIRE: AERIS AGILE TIP, AERIS AGILE TIP 300, CERTUS AGILE TIP, CERTUS...
Cardiovascular
262d
Cleared
Dec 20, 2013
PRESSUREWIRE AERIS AGILE TIP
Cardiovascular
29d
Cleared
Sep 05, 2013
PRESSUREWIRE
Cardiovascular
108d
Cleared
Oct 21, 2011
AO USB RECEIVER, WI-BOX, WI-BOX PSU KIT, WI-BOX XPRESS CABLE, PW USB RECEIVER
Cardiovascular
114d
Cleared
Feb 24, 2011
FEMOSTOP PLYS, FEMOSTOP HD, FEMOSTOP COMPRESSION ARCH
Cardiovascular
31d