Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K024278 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 710 Medtronic Parkway, Minneapolis, MN 5543... | 3 | 11/06/2007 | Medtronic Inc. Cardiac Rhythm Managment |
Medtronic Paceart 2004 Second Edition & Paceart 2005 First Edition versions of the Paceart Gateway S... | 3 | 05/31/2006 | Medtronic Inc. Cardiac Rhythm Managment |
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