Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K960983 |
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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® Everest® 20 Disposable Inflation Device, AC2200. Used to inflate/deflate balloon cath... | 2 | 08/25/2010 | Medtronic, Inc. |
Medtronic® Everest® 30 Disposable Inflation Device, AC3205P. Used to inflate/deflate balloon cat... | 2 | 08/25/2010 | Medtronic, Inc. |
Medtronic® Everest® 30 Disposable Inflation Device, AC3200. Used to inflate/deflate balloon cath... | 2 | 08/25/2010 | Medtronic, Inc. |
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