Medical Device Recalls
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1 result found
510(K) Number: K150582 |
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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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Stryker AutoPlex System. Model Numbers 0607-687-000, 0605-887-000, 0605-687-000, and 0605-683-000... | 2 | 08/15/2016 | Stryker Instruments Div. of Stryker Corporation |
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