Medical Device Recalls
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1 result found
510(K) Number: K130430 |
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Results per Page |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| 1. 11g/10mm iVAS System Kit, Product Number: 0705-310-000, UDI: (01)7613252505983; 2. 11g/15mm iVAS ... | 2 | 03/28/2018 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
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