St. Jude Medical, Daig Division, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
St. Jude Medical, Daig Division, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
St. Jude Medical, Daig Division, Inc. has 2 FDA 510(k) cleared medical devices. Based in Minnetonka, US.
Historical record: 2 cleared submissions from 2005 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by St. Jude Medical, Daig Division, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - St. Jude Medical, Daig Division, Inc.
2 devices