Medical Device Recalls
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1 result found
510(K) Number: K052459 |
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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 Adjustable Valve, 6248VAL, Sterilized using irradiation. Medtronic, Inc. Minneapolis, MN ... | 2 | 09/30/2008 | Medtronic Inc. Cardiac Rhythm Managment |
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