Medical Device Recalls
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1 result found
510(K) Number: K791963 |
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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 Mullins Transseptal Adult 7F, REF 008551. Intended for the introduction of cardiovascu... | 2 | 08/05/2013 | Medtronic Inc. Cardiac Rhythm Disease Management |
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