Medical Device Recalls
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1 result found
510(K) Number: K100254 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP) Catheter, catalog numbers D135... | 2 | 07/12/2018 |
FEI # 3009350690 Stryker Sustainability Solutions |
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