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St. Jude Medical / Daig Division

7 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
FastCath Transseptal Catheter Introducers with Hemostasis Valve, DAIG division of St. Jude recall (Z-0535-2007)St. Jude Medical / Daig Division2007-03-01
The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 6 recall (Z-0157-2007)St. Jude Medical / Daig Division2006-11-07
St. Jude AGILIS Steerable Introducer, Reorder number 408304 and 408308 (Australia). Steril recall (Z-1086-06)St. Jude Medical / Daig Division2006-06-03
Angio-Seal Vascular Closure Device. Ref 610109. 6F STS Platform. Sterilized by gamma radia recall (Z-0677-06)St. Jude Medical / Daig Division2006-03-25
Sheath Obturator, introducer, catheter. Obturator Accessory Kit Reorder number 406405, a 6 recall (Z-0125-06)St. Jude Medical / Daig Division2005-11-03
Telesheath Left Atrial Introducer System Right Superior. Telesheath Catheter Two-Piece Int recall (Z-1425-04)St. Jude Medical/Daig Division2004-09-01
Telesheath Left Atrial Introducer System Right Superior. Telesheath Catheter Two-Piece Int recall (Z-1426-04)St. Jude Medical/Daig Division2004-09-01

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