Medical Device Recalls
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1 result found
PMA Number: P980035/S014 |
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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 KAPPA 600/700/900 Series Implantable Pulse Generator (IPGs), Dual Chamber atrial sensing, ... | 1 | 06/11/2009 | Medtronic Inc. Cardiac Rhythm Disease Managment |
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