Medical Device Recalls
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1 result found
510(K) Number: K180834 |
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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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| Altrix® Precision Temperature Management System Model: 8001Product Usage: The Altrix system is int... | 2 | 10/24/2018 |
FEI # 1831750 Stryker Medical Division of Stryker Corporation |
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