St. Jude Medical, Daig Division, Inc. is one of 24544 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
Recent clearances: APEEL CS PLUS CATHETER DELIVERY SYSTEM, MODELS 407579, 407580, 407581, 407582, AGILIS STEERABLE CATHETER INTRODUCER, MODEL 408304
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