Medical Device Manufacturer · US , Minnetonka , MN

St. Jude Medical, Daig Division, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - St. Jude Medical, Daig Division, Inc. Cardiovascular ✕

2 devices

1-2 of 2

Cleared May 17, 2005

APEEL CS PLUS CATHETER DELIVERY SYSTEM, MODELS 407579, 407580, 407581, 407582

Cardiovascular · 18d

Cleared Jan 27, 2005

AGILIS STEERABLE CATHETER INTRODUCER, MODEL 408304

Cardiovascular · 122d